Glossary for Female sexual symptoms

Medical terms related to Female sexual symptoms or mentioned in this section include:

• $18p minus syndrome$: A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material that is missing.
• $3-Beta-HSD, Deficiency of$: A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wasting and abnormal sexual organ development depending on the level of deficiency.
• $3-Beta-Hydroxysteroid Dehydrogenase deficiency$: A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wasting and abnormal sexual organ development depending on the level of deficiency.
• $3-Beta-Hydroxysteroid Dehydrogenase, Type II, Deficiency of$: A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wasting and abnormal sexual organ development depending on the level of deficiency.
• $46,XX chromosome 7 deletion p13-p21$: A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities.
• $46,XX testicular DSD$: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
• $46,XX testicular disorder of sex development$: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
• $47,XXX syndrome$: A genetic condition where females have an extra X chromosome in each of their cells. Normally female cells have two X chromosomes. This is not usually an inherited condition but a defect that occurs during cell division. Often the condition is asymptomatic.
• AIDS-Related Opportunistic Infections: A term given to HIV patients who have a low CD4 count (below 200) which means that they have low levels of a type of immune cell called T-cells. AIDS patients tend to develop opportunistic infections and cancers. Opportunistic infections are infections that would not normally affect a person with a healthy immune system. The HIV virus is a virus that attacks the body's immune system.
• Abdominal Cancer: Growth of abnormal cells (tumour) affecting the organs in the abdominal cavity; may be due to primary growth of a tumour or spread from another tumour (metastases, secondary tumour)
• Abnormal uterine bleeding: The loss of blood from the uterus that varies from that which is considered normal
• Abnormal vaginal bleeding: refers to vaginal bleeding at any time during the menstrual cycle other than normal menstruation
• Abruptio placentae: A condition which is characterized by the premature detachment of the placenta from the uterus
• Achard-Thiers Syndrome: A rare hormonal disorder that occurs in diabetic postmenopausal women where body hair grows in a masculine manner. Hormonal therapy is used to correct the endocrine imbalance.
• Acquired prothrombin deficiency: A deficiency of prothrombin (vital for blood clotting) which is acquired through other conditions such as liver disease, anticoagulant drugs or vitamin K deficiency. The severity of symptoms is determined by the degree of deficiency.
• Acromegaly: An abnormal enlargement of the limbs due to increased secretion of growth hormone after the cessation of puberty
• Actinomycosis: A chronic infection usually caused by an organism normally found in human bowels and mouths. The disease usually affects the face and neck and results in deep, lumpy abscesses that emit a grainy pus through multiple sinuses.
• Acute (or transient) urinary incontinence: Acute (or Transient) Incontinence is caused by a new or recent medical problem that can be treated.
• Acute leukaemia of ambiguous lineage: A term used to describe a type of leukemia (a blood cancer) where the leukemic cells cannot be determined as myeloid or lymphoid or where both types of cells are present.
• Acute myeloblastic leukemia type 1: A form of blood cancer resulting in the rapid proliferation of immature blood cells (blast cells).
• Acute myeloblastic leukemia type 2: A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes.
• Acute myeloblastic leukemia type 3: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 3 involves the proliferation of promyelocytes.
• Acute myeloblastic leukemia type 6: A rare form of malignant bone marrow cancer involving the rapid proliferation of immature precursors of blood cells. Type 6 involves the proliferation of the immature precursors of red blood cells called erythroblasts.
• Acute myelocytic leukemia: A malignant cancer of blood-forming tissues resulting in a high number of immature leukocytes. Symptoms include soft bleeding gums, anemia, fatigue, fever, dyspnea, moderate splenomegaly, joint and bone pains and frequent infections. Also called acute granulocytic leukemia, acute myelogenous leukemia, acute nonlymphocytic leukemia, myeloid leukemia, splenomedullary leukemia, splenomyelogenous leukemia.
• Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent: The use of alkylating agents to treat cancer can result in leukemia in some patients.
• Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor: The use of topoisomerase type II inhibitors to treat cancer can result in leukemia in some patients.
• Acute myeloid leukaemia and myelodysplastic syndromes, therapy related: Certain cancer therapies can result in the development of leukemia in some patients. These therapies includes topoisomerase type II inhibitors and alkylating agents.
• Acute myeloid leukemia: A form of rapidly progressing blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
• Acute myeloid leukemia, adult: A form of blood cancer resulting in the rapid proliferation of granulocytes and monocytes, red blood cells and platelets.
• Acute promyelocytic leukemia: A rare bone marrow cancer characterized by a lack of mature blood cells and excessive amounts of immature blood cells (promyelocytes).
• Adenocarcinoma, Clear Cell: A type of cancer that occurs mainly in the genitourinary tract and the cells that make up the tumor are clear. It is very rare and most cases occur in females whose mothers used a drug called DES (synthetic estrogen) while pregnant.
• Adenomyosis: presence of ectopic endometrial tissue in the myometrium
• Adnexal and Skin Appendage Neoplasms: A type of tumour that develops on particular organs - eyes, skin and uterus. The tumors are usually benign but some may become malignant. The symptoms will vary depending on the location of the tumor and whether it is benign or malignant. These type of tumors tend to be most common in middle-aged women.
• Adnexal tenderness: Tenderness of the appendages or secondary structures of the uterus.
• Adrenal Cancer: A malignant cancer that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids. Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
• Adrenal Cortex Diseases: Diseases of the adrenal cortex. Examples includes Addison's disease, Cushing's syndrome and adrenal fatigue.
• Adrenal Cortex Neoplasms: A tumor that develops in the adrenal gland. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids.
• Adrenal Hyperplasia, Congenital (General): Congenital adrenal hyperplasia is an inherited condition characterized by adrenal insufficiency. It is caused by a deficiency in an enzyme needed to produce certain adrenal hormones such as cortisol and aldosterone.
• Adrenal adenoma, familial: A benign tumor that develops in the adrenal gland and tends to run in families. The tumor may be nonfunctioning (does not produce hormones) or functioning in which case excessive levels of hormones can cause a variety of symptoms depending on which hormone is involved. Adrenal hormones made in the cortex (outer part of the gland) are aldosterone, corticosteroids and androgenic steroids . Adrenalin and noradrenalin are the hormones made in the medulla (central part of the adrenal gland).
• Adrenal gland hyperfunction: Excessive activity of the adrenal gland which causes excessive production of one or more adrenal hormones (aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine). The increased adrenal gland activity may be caused by an adrenal gland tumor or by excessive stimulation of the gland. Pituitary hormones stimulate adrenal gland activity.
• Adrenal gland symptoms: Symptoms affecting the adrenal glands
• Adrenal hyperplasia, congenital type 3: A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency.
• Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency: A rare form of congenital adrenal hyperplasia characterized by a deficiency of 11-Beta-hydroxylase which results in excess androgen production and hypertension. The disorder can occur in virilizing, hypertensive and salt-wasting forms and symptoms may range from mild to severe.
• Adrenal hypoplasia congenital, X-linked: A genetic disorder which affects the body tissues that produce hormones. It is characterized by underdeveloped adrenal glands which results adrenal insufficiency and hypogonadotrophic hypogonadism.
• Adrenal incidentaloma: A tumor of the adrenal gland that is discovered incidentally while performing an imaging examination for reasons other than an adrenal tumor. The tumor may be asymptomatic or can causes excessive secretion of adrenal hormones and resulting symptoms. The tumor may also be malignant or benign.
• Adrenocortical carcinoma: A condition which is characterized by malignancy which affects the adrenocortex.
• Adrenoleukodystrophy: A rare hereditary metabolic disease that only occurs in male children and is characterized by adrenal atrophy and extensive cerebral demyelination causing progressive loss of mental functioning, aphasia, apraxia and sometimes blindness. The patient usually dies within 5 years.
• Aging: The medical conditions from getting older.
• Ahumada-Del Castillo Syndrome: A form of secondary amenorrhea often resulting from a pituitary gland tumor. The condition causes galactorrhea and amenorrhea even when the patient is not pregnant.
• Alcohol abuse: Excessive alcohol as a symptom of other conditions
• Allen-Masters syndrome: Damage to muscle layers in the pelvis which allows the abnormally increased movement of the cervix. It often occurs after a traumatic surgical birth, induced abortion or excessive vaginal packing.
• Allergic seminal vulvovaginitis: Vaginal inflammation following contact with semen after ejaculation.
• Amenorrhea: Absence of menstrual periods.
• Amphetamine abuse: Use of the stimulant drugs known as amphetamines or "speed"
• Androgen Insensitivity Syndrome: Females with male XY genetics but inability to respond to testosterone.
• Anemia, Iron-Deficiency: A lack of fully functioning red blood cells due to a deficiency of iron. The iron allows the body to make hemoglobin in red blood cells which in turn allows the red blood cell to carry oxygen.
• Anemia, Refractory, with Excess of Blasts: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. There are two types: type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a quarter of cases in type 1 and a third of cases in type 2.
• Anemia, Refractory, with Excess of Blasts, type 1: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a quarter of cases in type 1.
• Anemia, Refractory, with Excess of Blasts, type 2: A bone marrow disease which results in insufficient red blood cells in the blood (anemia). The prognosis is poor with death usually occurring within a couple of years. Type 1 refers to cases where the level of blasts is less than 10% and type 2 refers to cases where the level of blasts is 10-20%. When too many immature blood cells (blasts) are produced by the bone marrow, the condition may progress to acute myeloid leukemia - occurs in about a third of cases in type 2.
• Angular cheilitis: This is an inflammation with maceration, exudation and fissure formation at the labial commissures
• Anorexia: This is known as a lack of or loss of appetite for food
• Anorexia Nervosa: A disorder where a distorted sense of body image leads to self-starvation to the point of death in some cases.
• Anorexia nervosa, genetic types: There is mounting evidence that anorexia nervosa may be caused by genetic factors which when combined with psychosocial factors can increase a persons risk of developing the condition.
• Aplastic anemia: A blood disorder where the bone marrow produces insufficient new blood cells.
• Asherman's syndrome: Scarring and adhesions that develop in the uterus and can result in menstrual and fertility problems.
• Atrophic vaginitis: Type of vaginitis usually related to aging and menopause
• Attenuated congenital adrenal hyperplasia: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
• Autoimmune Endometriosis: An endometriosis that is caused by an autoimmune reaction
• Autoimmune Hepatitis: Liver inflammation caused due to autoimmune processes where the body's immune system attacks the liver.
• Autoimmune Thrombocytopenia: Autoimmune disorder causing a lack of blood platelets.
• Autoimmune oophoritis: An autoimmune condition where the body's own immune system attacks the ovaries and causes them to become inflamed. It can lead to ovarian function stopping prematurely.
• Autoimmune thyroid disease associated Celiac Disease: Patients with autoimmune thyroid disease are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Autoimmune thyroid diseases: Autoimmune diseases of the thyroid gland.
• Autonomic neuropathy: A condition which is characterized by a functional disturbance or pathological change in the autonomic nervous system
• BXO: Skin condition of the penis which can effect the glans, prepuce or urethra.
• Bacterial toxic-shock syndrome: A very rare, potentially fatal infection caused by toxins produced by bacteria, especially bacteria such as Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources.
• Bardet-Biedl syndrome, type 1: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 1 is caused by a defect in chromosome 11q13.
• Bardet-Biedl syndrome, type 10: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 10 is caused by a defect in chromosome 12q.
• Bardet-Biedl syndrome, type 11: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 11 is caused by a defect in chromosome 9q33.1.
• Bardet-Biedl syndrome, type 12: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 12 is caused by a defect in chromosome 4q27.
• Bardet-Biedl syndrome, type 2: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 2 is caused by a defect in chromosome 16q21.
• Bardet-Biedl syndrome, type 3: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 3 is caused by a defect in chromosome 3p12-q13.
• Bardet-Biedl syndrome, type 4: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 4 is caused by a defect in chromosome 15q22.3.
• Bardet-Biedl syndrome, type 5: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 5 is caused by a defect in chromosome 2q31.
• Bardet-Biedl syndrome, type 6: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 6 is caused by a defect in chromosome 20p12.
• Bardet-Biedl syndrome, type 7: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 7 is caused by a defect in chromosome 4q27.
• Bardet-Biedl syndrome, type 8: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 8 is caused by a defect in chromosome 14q32.11.
• Bardet-Biedl syndrome, type 9: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 9 is caused by a defect in chromosome 7p14.
• Bartholin's abscess: Abscess in a small vaginal gland
• Bartholin's cyst: Cyst in a small vaginal gland
• Bearn-Kunkel syndrome: A type of autoimmune liver disease characterized by liver damage, very high blood gammaglobulin levels and increased plasma cells.
• Bernard-Soulier Syndrome: A congenital bleeding disorder marked by inability of platelets to coagulate or by insufficient platelets. The platelets that are present are often large.
• Biemond syndrome type 2: A rare inherited condition characterized by mental retardation, obesity, polydactyly and underdeveloped genitals.
• Bleeding after sex: Vaginal bleeding after sexual intercourse
• Bleeding symptoms: Any type of bleeding symptoms.
• Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fertility problems whereas type 1 only involves the eye anomalies.
• Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome, type 1: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid. The severity of symptoms is variable. There are two subtypes of the condition: Type 2 involves eye anomalies as well as female fertility problems whereas type 1 only involves the eye anomalies.
• Blepharophimosis, ptosis, epicanthus inversus: A rare genetic disorder characterized by inner canthal folds, lateral displacement of inner canthi and drooping upper eyelid.
• Bloody vaginal discharge: discharge from the vagina other than normal menstruation
• Boucher-Neuhauser syndrome: A very rare disorder characterized by spinocerebellar ataxia, eye abnormalities and a failure of the pituitary to stimulate gonadal development during puberty.
• Breast Feeding: Nursing an infant with breast milk.
• Breisky disease: A progressive wasting disease of the vulva that occurs in postmenopausal women and is probably caused by hormonal imbalance.
• Brenner tumor of the vagina: A Brenner tumour usually occurs in the ovaries but can sometimes occur in the vagina. The tumor is generally benign.
• Bulimia nervosa: Eating disorder with binging (overeating) and purging (vomiting).
• CCFDN: A rare, recessively inherited syndrome characterized by cataracts during infancy, unusual facial appearance and neuropathy.
• Candidiasis: Fungal infection of moist areas such as mouth or vagina
• Cardiomyopathy, hypogonadism, collagenoma syndrome: A rare inherited condition characterized primarily by skin nodules. The skin nodules may be associated with organ system involvement resulting in a variety of other symptoms.
• Celiac Disease: Digestive intolerance to gluten in the diet.
• Celiac disease, susceptibility to 1: The susceptibility to developing celiac disease due to a genetic defect on chromosome 6p21.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 10: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q25-q26. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 11: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3q28. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 12: The susceptibility to developing celiac disease due to a genetic defect on chromosome 6q25.3. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 13: The susceptibility to developing celiac disease due to a genetic defect in the SH2B3 gene on chromosome 12q24. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 2: The susceptibility to developing celiac disease due to a genetic defect on chromosome 5q31-q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 3: The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q33. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 4: The susceptibility to developing celiac disease due to a genetic defect on chromosome 19p13.1. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 5: The susceptibility to developing celiac disease due to a genetic defect on chromosome 15q11-q13. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 6: The susceptibility to developing celiac disease due to a genetic defect on chromosome 4q27. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 7: The susceptibility to developing celiac disease due to a genetic defect on chromosome 1q31. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 8: The susceptibility to developing celiac disease due to a genetic defect on chromosome 2q11-q12. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Celiac disease, susceptibility to 9: The susceptibility to developing celiac disease due to a genetic defect on chromosome 3p21. Celiac disease is a small intestine disorder where the ingestion of foods containing wheat gluten and similar proteins leads to the inflammation of the small intestine lining. This damage affects absorption of nutrients and can cause symptoms such as diarrhea. Growth in children due to malabsorption may also result. The type and severity of symptoms is variable.
• Cephalothoracic progressive lipodystrophy: A rare acquired disorder that involves adipose tissue abnormalities and is characterized by loss of adipose tissue mainly in the trunk and arms.
• Cervical Intraepithelial Neoplasia: Dysplasia of the cervical epithelium often premalignant.
• Cervical cancer: A condition which is characterized by the occurrence of malignancy on the cervix
• Cervical dilation: Dilation of the cevix.
• Cervical erosion: A shallow superficial ulceration of the cervix.
• Cervical polyps: Benign polyps on the cervix of the uterus
• Cervicitis: A condition which is characterized by inflammation of the cervix
• Cervix symptoms: Symptoms affecting the cervix
• Chancroid: An sexually transmitted disease caused by the Haemophilus ducreyi bacteria and is characterized by painful genital ulceration.
• Chapple syndrome: A rare birth disorder characterized by painful menstruation, knees bent back and a uterus that is tilted backwards (retroverted). It is believed to be caused by an abnormal fetal position inside the womb.
• Chiari-Frommel syndrome: A hormonal disorder where a woman continues to produce milk even after the child has been weaned.
• Chlamydia: Common sexually transmitted disease often without symptoms.
• Choriocarcinoma: Rare cancer of the placenta
• Chromosome 15q duplication syndrome: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
• Chromosome 15q, trisomy: A rare chromosomal disorder involving an extra copy of genetic material from the long arm of chromosome 15. The type and severity of symptoms are determined by the amount and location of the duplicated genetic material.
• Chromosome 17p, partial deletion: A rare chromosomal disorder involving deletion of genetic material from the short arm of chromosome 17. The type and severity of symptoms are determined by the amount and location of the lost genetic material.
• Chromosome 18q, partial deletion: A rare chromosomal disorder involving deletion of genetic material from the long arm of chromosome 18. The type and severity of symptoms are determined by the amount and location of the lost genetic material.
• Chromosome 6q duplication syndrome: A rare chromosomal disorder involving duplication of the long arm (q) of chromosome 6 which results in various abnormalities depending on the size and location of the portion of duplicated genetic material.
• Chromosome 7, Partial Deletion of Short Arm: A rare chromosomal disorder where part of the short arm (p) of chromosome 7 is deleted resulting in various abnormalities which are determined by the size and location of the deleted portion.
• Chromosome 7, partial monosomy 7p: A rare chromosomal disorder where part of the short arm (p) of chromosome 7 is deleted resulting in various abnormalities which are determined by the size and location of the deleted portion.
• Chromosome 8 recombinant syndrome: A rare recombinant chromosomal disorder involving chromosome 8 which results in various abnormalities.
• Chromosome 9 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities.
• Chromosome 9, trisomy: A rare chromosomal disorder where there are three copies of chromosome 9 in the body's cells instead of the normal two resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated.
• Chromosome 9p tetrasomy syndrome: A rare chromosomal disorder where there is four copies of the short arm of chromosome 9 instead of the normal two resulting in various abnormalities.
• Chronic Kidney Disease: Long-term and generally irreversible disease of the kidneys due to infection, obstruction, congenital diseases or generalised diseases causing failure of the kidneys' normal functions.
• Chudley syndrome 1: A rare syndrome characterized by mental retardation, obesity, hypogonadism and a distinctive mouth.
• Clitoris itch: An sensation to scratch the clitoris
• Clitoris pain: A feeling of distress and agony caused by the stimulation of pain nerve endings in the clitoris.
• Clitoris rash: An eruption on the skin of the clitoris.
• Clitoris symptoms: Symptoms affecting the clitoris
• Collagenous celiac disease: Collagenous celiac disease is used to describe progressive celiac disease characterized by the presence of a layer of collagen (scarring) in the intestinal layers. This form of celiac disease usually fails to respond to treatments such as gluten-free diets. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition usually fails to respond to treatment and has a poor prognosis.
• Congenital adrenal hyperplasia: A condition where excessive secretion of adrenocortical androgens cause a somatic masculization or ?virilization? effect on a fetus or baby. Symptoms in girls may include masculization of sex organs, low voice, acne, amenorrhea and masculine hair distribution and muscle growth. Symptoms in boys include enlarged penis, small testes. Children with the condition are usually taller than average but develop into short adults. Also called adrenogenital syndrome or adrenal virilism.
• Congenital adrenal hyperplasia - non-classical form: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
• Congenital adrenal hyperplasia - simple virilizing form in females: A group of disorder that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The simple virilizing form involves a moderate deficiency of 21-hydroxylase and differs in its effects on males and females.
• Cortisone reductase deficiency: An inborn error of steroid metabolism due to a deficiency of an enzyme called cortisone reductase (11-beta-hydroxysteroid dehydrogenase). This enzyme is needed to convert cortisone to cortisol.
• Cushing syndrome, familial: A hormonal disorder caused by high levels of the cortisol hormone due to the abnormal development of the adrenal gland.
• Cushing-like symptoms: Symptoms similar to those of Cushing's disease
• Cystic Fibrosis: Cystic fibrosis is a hereditary disease affecting the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure.
• Cystocele: Bladder falls down into the vagina.
• De la Chapelle syndrome: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
• Deafness hypogonadism syndrome: A rare condition characterized by the combination of hypogonadism and deafness.
• Depressive symptoms: Inappropriate depressed mood.
• Dermoid cyst: Benign cystic tumor often containing skin, hair, and other tissue
• Diabetes-like symptoms: Symptoms similar to those of diabetes
• Diabetic neuropathy: nerve damage which maybe motor, sensory and autonomic
• Diethylstilbesterol - Teratogenic Agent: There is strong evidence to indicate that the use of Diethylstilbesterol during pregnancy may cause a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposure and the stage of pregnancy that the exposure occurred at.
• Double uterus-hemivagina-renal agenesis: A very rare malformation of the uterus and vagina.
• Down's syndrome associated Celiac Disease: Patients with Down's syndrome have a high degree of susceptibility to developing celiac disease. Up to 17% of Down's syndrome sufferers develop celiac disease but this rate varies amongst age groups and country of origin. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Dysfunctional Uterine Bleeding: Uterus bleeding unrelated to periods
• Dysmenorrhea: Excessive menstrual-like cramping pain
• Dyspareunia: Painful sexual intercourse
• Dystrophia myotonica 1: A rare genetic disorder characterized by myotonia, muscle atrophy, cataracts and hypogonadism.
• Eating symptoms: Symptoms related to eating.
• Edwardsiella tarda infection: A type of bacterial infection. The bacterium (Edwardsiella tarda) infects freshwater-dwelling animals and transmission occurs through consuming infected animals or contact with contaminated water. Symptoms are determined by the location of the infection. Healthy people are often able to fight of the infection but those with an underlying illness or poor immune systems may be more susceptible.
• Ehlers danlos syndrome: An inherited disorder of the connective tissue causing it to become weak and fragile. Connective tissue is found in skin, muscles, tendons and ligaments and hence all of these may be affected by weakness
• Endometrial Cancer: Cancer of the endometrium (uterus lining).
• Endometrial conditions: Conditions that affect the female endometrium that is located in the uterus
• Endometrial hyperplasia: Thickening of the endometrium (lining of the uterus)
• Endometrial stromal sarcoma: A rare type of cancer that develops from the endometrial layer of the uterus. The cancer may be slow-growing or aggressive and may metastasize.
• Endometriosis: Misplaced uterus tissue causing scar tissue.
• Endometritis: Inflammation of the endometrium (uterine lining)
• Enlarged ovaries: Where the ovaries of a female have increased in size to what is considered normal
• Enlarged ovary: An enlargement of the female ovary to a size bigger than considered normal
• Ewing's family of tumors: A rare condition where tumors develop in bone or soft tissue. Usually teenagers are affected.
• Excessive dieting: Excessive limitation of food intake can lead to problems and effects such as dizziness, depression, intestinal problems, edema and impaired growth.
• Excessive menstrual bleeding: A condition which is characterized by an abnormal excess of blood loss during menstruation
• Factor V and factor VIII, combined deficiency of: A rare inherited blood disorder where a deficiency of Factor V and factor VIII results in bleeding problems. Factor V and factor VIII is involved in blood coagulation.
• Factor V deficiency: An inherited disorder where the deficiency of a blood component affects its ability to clot properly which can lead to bleeding problems. The severity of the disorder can vary from easy bruising to life-threatening hemorrhages.
• Factor X deficiency: A rare blood clotting disorder which may be inherited or acquired in people suffering from conditions such as liver disease, amyloidosis, leprosy and certain cancers. The underlying cause is the deficiency of a protein (Factor X) which is needed for the blood to clot properly. The condition may cause mild to severe bleeding depending on the degree of deficiency of Factor X.
• Factor X deficiency - Friuli: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Fruili variant tends to only cause moderate bleeding problems and occurs mainly in an area of Italy called Fruili.
• Factor X deficiency - Kanazawa: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Kanazawa variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Ketchikan: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Ketchikan variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Nottingham: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Nottingham variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Padua: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Padau variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - San Antonio: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The San Antonia variant results in 14% of normal Factor X blood clotting activity.
• Factor X deficiency - Santo Domingo: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Santo Domingo variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Shanghai: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Shangai variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - St. Louis II: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The St. Louis II variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Stockton: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Stockton variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Taunton: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Taunton variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Tokyo: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Tokyo variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Vorarlberg: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Vorarlberg variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Wenatchee I: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Wenatchee I variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - Wenatchee II: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The Wenatchee II variant results in reduced Factor X blood clotting activity.
• Factor X deficiency - autosomal dominant: A rare inherited blood clotting disorder where there is a deficiency of a protein (Factor X) which is needed for the blood to clot properly. The autosomal dominant variant results in reduced Factor X blood clotting activity.
• Factor XIII Deficiency: A very rare inherited or acquired blood disorder caused by a deficiency of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
• Factor XIII deficiency, congenital: A very rare inherited blood disorder caused by a deficiency of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
• Factor XIII, A1 subunit Deficiency: A very rare inherited or acquired blood disorder caused by a deficiency of subunit A of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
• Factor XIII, B subunit Deficiency: A very rare inherited or acquired blood disorder caused by a deficiency of subunit B of Factor XIII which is involved in stabilizing blood clot formation. The condition manifests as bleeding problems.
• Fallopian tube cancer: A cancer that originates in the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon.
• Fallopian tube conditions: Conditions that affect the fallopian tubes of a woman
• Fallopian tube symptoms: Symptoms affecting the female fallopian tubes
• Familial hypopituitarism: Impaired pituitary gland hormone-producing activity that tends to run in families. The failure of the pituitary gland in turn affects other hormone-producing glands which rely on the hormones from the pituitary gland for their activity. Symptoms are determined by the degree and type of hormone deficiency involved.
• Female genital disorders: Any condition affecting the female genital organs.
• Female infertility: A condition characterized by the inability of a female to become pregnant
• Female pseudohermaphrodism - anorectal anomalies: A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies.
• Female reproductive toxicity: There is mounting evidence which indicates that exposure to certain agents may produce adverse reproductive or fetal developmental effects. The possible range of effects includes reduced fertility, low birth weight, childhood cancer, spontaneous abortion and birth defects. Agents which may be implicated in these adverse effects includes anticancer drugs, carbon disulfide, carbon monoxide, lead, pesticides, organic solvents and tobacco smoke.
• Female reproductive toxicity - Dioxins: There is limited conflicting evidence which indicates that some women exposed to dioxins may suffer adverse effects as a result. Spontaneous abortion and menstrual disorders and birth defects are the possible adverse effects.
• Female sexual conditions: Sexual conditions that affect the female
• Fistula: The abnormal passage between two internal organs
• Fitz-Hugh-Curtis syndrome: A rare condition where the thin layer around the liver becomes infected as a result of a spread of infection from gonococcal or chlamydial infections in females.
• Florid cystic endosalpingiosis of the uterus: Benign tumor-like uterine cysts.
• Forbes-Albright syndrome: A rare condition where a hormone secreting pituitary or hypothalamic tumor causes galactorrhea and amenorrhea.
• Fowler-Christmas-Chapple syndrome: A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve.
• Fragile-X Syndrome: A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females.
• Fraser Syndrome: A rare disorder characterized by the absence of one or both eyes as well as any of a number of other possible congenital abnormalities. Up to half of cases are stillborn.
• Fraser-like syndrome: A very rare syndrome characterized by fused eyelids, airway anomalies, cysts in the ovaries and finger and toe abnormalities.
• Fryns Syndrome: A rare genetic disorder characterized by diaphragmatic abnormalities, coarse face and abnormal growth or development of ends of fingers and toes.
• Functioning pancreatic endocrine tumor: Tumors that develop in the pancreas and cause excessive secretion of one or more pancreatic hormones such as insulin, somatostatin, glucagons, gastrin, ACTH (corticosteroids) and vasoactive intestinal peptidase.
• GAPO syndrome: A rare condition characterized by retarded growth, alopecia, otpic atrophy and failure of teeth to erupt.
• Galactorrhea: This is where there is an excessive or spontaneous flow of milk from the female breast
• Galactorrhoea-Hyperprolactinaemia: Increased blood prolactin levels associated with galactorrhea (abnormal milk secretion). It may be caused by such things as certain medications, pituitary disorders and thyroid disorders. The condition can occur in males as well as females.
• Genital herpes: Sexually transmitted infection of the genital region.
• Genital warts: Skin warts in the genital regions.
• German syndrome: A rare disorder caused by fetal exposure to trimethadione (anticonvulsant drug) and resulting in various physical and developemental abnormalities.
• Gestational trophoblastic tumor: A rare tumor that develops in the uterus from cells formed after an abnormal conception (abnormal union of sperm and egg cell). Gestational trophoblastic tumors can also develop from a normal placenta. There are two type of gestational trophoblastic tumors: choriocarcinoma and hydatidiform mole.
• Gigantism: Gigantism refers to abnormally high linear growth due to excessive action of insulin-like growth factor-I (IGF-I) while the epiphyseal growth plates are open during childhood.
• Glassy cell carcinoma of the cervix: A rare type of cervical cancer.
• Gonadal dysgenesis: The abnormal development of gonads which means that the sex hormones are not being produced. The gonads are the primary reproductive organs - testes in males and ovaries in females. These organs produced sperm and eggs as well as sex hormones - testes produce the male hormone called testosterone and ovaries produce the female hormone called estrogen. Abnormal gonad development and hence lack of sex hormones can affect sexual differentiation between males and females and puberty may be delayed or fail to occur altogether.
• Gonadal dysgenesis Turner type: The abnormal development of gonads that occurs in Turner syndrome due to a chromosomal abnormality. It occurs when the there is only one fully functioning X chromosome instead of two which results in underdeveloped female characteristics. The severity of symptoms is determined by how much of the second sex chromosome is missing.
• Gonadal dysgenesis mixed: A rare condition where the testes develop abnormally with asymmetrical gonads as well as sex chromosome abnormalities. The physical manifestations may range from development of female genitalia to male genitalia with hypospadias.
• Gonadal dysgenesis, XX type: A rare genetic condition involving non-functional ovaries causing a failure of puberty due to the lack of production of sex hormones by the ovaries.
• Gonorrhea: Common sexually transmitted disease often without symptoms.
• Granuloma inguinale: Granulomous disease spread sexually.
• Graves disease: A condition which is an autoimmune disease that affects the thyroid resulting hyperthyroidism
• Gulf War syndrome: Syndrome in military veterans of the Gulf war
• Gynaecological conditions: Any condition the affects the female reproductive organs
• Gynandroblastoma: A type of ovarian tumor that causes feminizing and masculinizing effects of estrogen and androgen.
• HAIR-AN Syndrome: A very rare syndrome that affects females only and is characterized mainly by insulin resistance, dark velvety patches of skin and increased male hormone production in females.
• HIV/AIDS: HIV is a sexually transmitted virus and AIDS is the progressive immune failure that HIV causes.
• Habitual abortion: The occurrence of two or more spontaneous abortions in a row. The condition may result from severe fetal abnormality, endocrine disorders, severe kidney problems, structural defects of the cervix or uterus or immune problems.
• Halal Setton Wang syndrome: A very rare syndrome characterized mainly by eye, teeth, nail and skin abnormalities.
• Hashimoto's thyroiditis: A progressive disease of the thyroid which leads to degeneration and hypothyroidism
• Heavy menstruation: When there is more than usual blood loss during menstruation
• Heavy periods: Excessive menstrual bleeding (called menorrhagia or hypermenorrhea)
• Hemorrhagic thrombocythemia: A rare blood disorder characterized by increased number of platelets in the blood which often results in an enlarged spleen, bleeding and blood vessel blockages.
• Hepatocellular carcinoma (fibrolamellar variant): A rare form of liver cancer. The prognosis for this variant of hepatocellular cancer is better than for hepatocellular cancer.
• Herbal Agent overdose - Cottonseed: Cottonseed can be used as a herbal agent used to reduce male fertility in China. The herbal agent contains a chemical called gossyphol which can cause various overdose symptoms if ingested in excessive quantities.
• Hereditary Leiomyomatosis and Renal Cell Cancer: A rare inherited condition characterized by the presence of tumors that develop from smooth muscle tissue in the skin, uterus and the kidneys. The skin anomalies can occur on any part of the body and gradually increase in number and size with age. Kidney tumors develop in only a relatively small proportion of patients with the condition.
• Hereditary hemorrhagic telangiectasia: A rare genetic disorder characterized by epistaxes and multiple telangiectases.
• Hereditary hypothyroidism: Hereditary hypothyroidism is a condition in which there is a defect in the thyroid gland which leads to increased production of TSH reduced production of thyroid hormone.
• Human Papillomavirus: Very common sexually transmitted disease causing genital warts and associated with certain cancers.
• Human carcinogen - Infection with Human papillomavirus type 16: Infection with Human papillomavirus type 16 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 18: Infection with Human papillomavirus type 18 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 31: Infection with Human papillomavirus type 31 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 35: Infection with Human papillomavirus type 35 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 39: Infection with Human papillomavirus type 39 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 45: Infection with Human papillomavirus type 45 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 51: Infection with Human papillomavirus type 51 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 52: Infection with Human papillomavirus type 52 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 56: Infection with Human papillomavirus type 56 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 58: Infection with Human papillomavirus type 58 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 59: Infection with Human papillomavirus type 59 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Human carcinogen - Infection with Human papillomavirus type 66: Infection with Human papillomavirus type 66 is deemed to be carcinogenic to humans. Infection with the virus does not mean the patient will definitely develop cancer but the risk of cancer is increased.
• Hydatidiform mole: A rare condition where an abnormal union between an egg and a sperm results in the formation of grape-like cysts instead of a baby. The growth is not malignant.
• Hyperadrenalism: Excessive levels of adrenal hormones in the body. Symptoms depend on which hormone is involved and the degree of involvement. Adrenal hormones are aldosterone, corticosteroids, androgenic steroids, epinephrine and norepinephrine.
• Hypergonadotropic ovarian failure: Premature onset of menopause - occurs before the fourth decade -average age of onset of menopause is about 50 years of age. The condition can occur sporadically or may be inherited in a familial manner.
• Hypergonadotropic ovarian failure, familial or sporadic: A rare disorder where the ovaries fail to function prematurely. Ovarian failure can occur in the 20's or 30's. Normal ovarian failure occurs during menopause. Premature ovarian failure can be caused by a genetic mutation and can occur sporadically or in a familial pattern.
• Hyperprolactinemia: High levels of prolactin in the blood.
• Hyperthyroidism: The excessive activity of the thyroid gland
• Hypogonadism - retinitis pigmentosa: A very rare syndrome characterized by eye disease (retinal pigmentosa) and the absence of puberty caused by a deficiency of hormones that stimulate the sex organs (gonads) into producing the hormones that initiate puberty.
• Hypothyroid goitre: Goitre is the enlargement of the thyroid gland and hypothyroid state is characterized by increased TSH levels and decreased T3 and T4 levels circulating in the body.
• Hypothyroidism: The decreased activity of the thyroid gland
• Ichthyosis male hypogonadism: A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads.
• Imperforate hymen: Lack of opening in the vaginal hymen
• Inflammatory pelvic pain: Inflammatory pelvic pain can be chr, cyclic,non cyclic, localized of generalized, or a combination. It affects women of reproductive age and older. It's important to note that sudden, severe pain with mass indicates a serious disorder such as an ectopic pregnancy, and it also requires immediate evaluation and treatment.
• Interstitial cystitis: A rare condition involving inflammatory disease of the bladder which progresses slowly.
• Kallmann Syndrome: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance.
• Kallmann syndrome 2: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 2 is caused by a genetic defect located at chromosome 8p11.2-p11.1.
• Kallmann syndrome, type 1, X-linked: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 1 is caused by a genetic defect located at chromosome Xp22.3.
• Kallmann syndrome, type 3, recessive: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 3 is recessively inherited and the genetic defect is located at chromosome 20p13.
• Kallmann syndrome, type 4: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 4 is caused by a genetic defect located at chromosome 3p21.1.
• Lactotroph adenoma: A benign pituitary tumor that secretes excessive prolactin which can affect the functioning of the reproductive system - testes and ovaries. The tumor may also grow large enough to compress adjacent structures such as the eye nerves.
• Laron syndrome type 1: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
• Laron syndrome type 2: Laron syndrome is a rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results. Type 1 involves a defect in the growth hormone receptor gene which prevents the hormone from binding and being used. Hence there are high levels of free growth hormone in the plasma. Type II involves a problem with the processing of the growth hormone once it has been bound properly to the cell surface.
• Laron-type dwarfism: A rare genetic disease where the body has sufficient growth hormones but lacks receptors to utilize the hormone and hence dwarfism results.
• Late start of menstruation: Late first period in adolescent girls
• Laurence-Moon Syndrome: A rare inherited disorder characterized by vision loss, impaired hormone production, mental retardation and spastic paraplegia.
• Leiomyomatosis, Esophagogastric and Vulvar: A rare condition where a tumor develops in the esophagus and vulva. The condition appears to be inherited in an autosomal dominant manner.
• Leukemia, Myeloid: A form of blood cancer that causes a proliferation of the precursors or immature red blood cells, platelets and certain white blood cells such as granulocytes and monocytes.
• Leukemia, Myeloid, Aggressive-Phase: Myeloid leukemia is a form of cancer where the bone marrow makes too many myeloid cells (granulocytes and their precursors) in the bone marrow which accumulates in the blood and eventually invades various parts of the body. The aggressive phase of myeloid leukemia follows the chronic form and is a sign that the condition is progressing more rapidly to a blast crisis which is the final stage of leukemia.
• Lichen planus: Skin rash
• Lichen sclerosis: Disease causing leathery or dry skin in genital areas.
• Light periods: Unusually light menstrual bleeding
• Lipodystrophy, familial partial, type 3 (FPLD3): A rare metabolic disorder involving abnormal fat gradually disappears from the limbs, trunk and buttocks but stays the same or accumulates on areas such as the face, shoulders, neck and genitals.
• Lubs syndrome: A rare condition where a genetic male is unable to respond to male hormones (androgen) which results in the development of female physical characteristics.
• Lundberg II syndrome: A rare syndrome involving cataracts, reduced hormone production by ovaries or testes and myopathy which mainly involves the facial and muscles close to the trunk.
• Lymphogranuloma venereum: Type of chlamydia (sexually transmitted disease)
• Male reproductive toxicity - Benzene: Exposure to Benzene, a recognized reproductive toxicant, can negatively affect the male reproductive system. Benzene is a widely used chemical - in pesticides and as a solvent in industries such as pesticide manufacturing, laboratory chemicals, printing, paper and pulp manufacture and pharmaceuticals manufacture. The severity and nature of the adverse effect is variable and can be influenced by factors such as level of exposure and individual sensitivity to the chemical. Effects on the male reproductive system can include such things as altered sexual behavior, altered fertility and problems with sperm shape or count.
• Malignant mixed Mullerian tumor: A rare malignant cancer that develops in the uterus, ovary or fallopian tubes. The tumor contains epithelial and stromal cells. The cancer may be slow-growing or aggressive and may metastasize.
• Marijuana abuse: Illicit depressant/hallucinogenic drug
• Martsolf syndrome: A rare inherited condition characterized by mental retardation, cataracts, small head and hypogonadism (reduced production of hormones by ovaries or testes).
• Masculinisation: Increased male physical appearance in females
• McCune-Albright Syndrome: A rare genetic multisystem disorder characterized by abnormal skin pigmentation and endocrine gland dysfunction and replacement of parts of bone tissue with fibrous material.
• Menopause: End of female reproductive years
• Menorrhagia: Excessive or prolonged blood loss during menstruation
• Menstrual changes: Any change to a females usual menstrual cycle
• Menstrual conditions: Any condition that is associated with the female menstrual cycle
• Menstrual cramps: Pelvic or other menstrual-related pains
• Menstrual disorders: Any medical condition which alters a womans menstrual cycle from normal
• Menstrual irregularities: Various abnormalities of periods and menstruation.
• Menstrual pain: Pain that occurs with menstruation
• Menstruation: The passage of blood and uterine tissue through the vagina cyclically
• Metrorrhagia: Bleeding occurring at irregular intervals between periods.
• Miscarriage: Symptoms related to miscarriage or stillbirth.
• Missed period: When a female you is menstruating fails to menstruate when expected
• Mittelschmerz: Mid-cycle abdominal pain due to ovulation
• Mullerian aplasia: A birth defect involving the absence of the uterus, cervix and top part of the vagina but normal external genitals and ovarian function. Secondary sexual characteristics generally develop normally but menstruation is absent.
• Multiple endocrine neoplasia type 1: Rare inherited disease causing tumors in multiple glands
• Myoma (fibroid): A benign tumour of the muscle in the wall of the uterus.
• Nathalie syndrome: A very rare condition described in four children of one family. The condition is characterized by wasting of the spine muscles, abnormal heart electrical activity, cataracts, hypogonadism and hearing impairment.
• Neurodermatitis: Lichen simplex chronicus refers to thickened itchy skin that results from persistently rubbing or scratching an area of skin.
• Neuroendocrine carcinoma of the cervix: A rare form of cervical cancer which tends to be quite aggressive.
• Neurosarcoidosis: A rare disorder involving sarcoidosis of the nervous system. Sarcoidosis is a chronic inflammatory disorder that can affect virtually any part of the body. Neurosarcoidosis involves inflammation and abnormal deposits in parts of the nervous system including the brain and spinal cord which affects their functioning. Symptoms may be sudden and severe or may be mild and progress slowly. Symptoms are determined by the degree of nerve involvement.
• Non Classic Congenital Adrenal Hyperplasia: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
• Non-Specific Urethritis: Urethral infection usually sexually transmitted
• OHSS: Excessive stimulation of the ovaries that usually occurs as a complication of in vitro fertilization but may also occur spontaneously. The degree of excessive ovarian stimulation may vary from mild to severe.
• Oligomenorrhoea: Periods occurring infrequently, with time between periods varying from 35 days to 6 months.
• Ovarian cancer: A condition which is characterized by a malignancy that is located in the ovary
• Ovarian carcinosarcoma: A type of ovarian cancer.
• Ovarian cyst: A cyst which is located in the ovary
• Ovarian cysts: Cysts which are located in the ovaries
• Ovarian insufficiency due to FSH resistance: A rare disorder where the ovaries fail to function normally as they are unable to respond to follicle stimulating hormones.
• Ovarian insufficiency, familial: A rare inherited disorder where the ovaries fail to function normally despite normal levels of hormones that stimulate ovarian activity. Ovarian failure is a normal phase of aging and is associated with menopause but it is termed ovarian insufficiency when it occurs in a female under the age of 40.
• Ovarian tumour: A tumour that is located on the ovary.
• Ovarioleukodystrophy: A rare syndrome characterized by ovarian failure and degeneration of the brain white matter which causes mental and motor problems.
• Ovary conditions: Any condition that affects a female ovary
• Ovary symptoms: Symptoms affecting the ovaries
• Painful intercourse: Pain during sexual intercourse
• Painful menstruation: The association of pain with menstruation
• Painful sexual intercourse: The experience of pain whilst having sexual intercourse
• Panhypopituitarism: A rare condition where all pituitary hormones are absent or reduced. The condition may be congenital or acquired through such things as pituitary tumors. The pituitary gland regulates the activity of other endocrine glands as well as controlling growth. Other endocrine glands include adrenal, parathyroid, thyroid, pancreas, ovaries and testes. Symptoms can vary greatly depending on the degree of deficiency of the various hormones.
• Partial 7p Monosomy: A rare chromosomal disorder where part of the short arm (p) of chromosome 7 is deleted resulting in various abnormalities which are determined by the size and location of the deleted portion.
• Pelvic Cancer: Any malignancy that is located in the anatomical location of the pelvis
• Pelvic inflammatory disease: A condition which is characterized by an infection which is located in the upper female genital tract
• Pelvis conditions: Any condition that affects the pelvis
• Perimenopause: The start of onset of menopause
• Peritoneum cancer: A condition that is characterised by the location of a malignant lesion in the perineum
• Peritoneum disorders: Any condition that affects the peritoneum
• Persistent sexual arousal syndrome: A sexual disorder where genital arousal in females continues even though there is no real interest in sex. Patients can find the condition very traumatic as even orgasm does nothing to alleviate the symptoms.
• Pinworm: Small, threadlike parasitic worms mainly in colon and rectum
• Pituitary Cancer: Cancer of the pituitary gland.
• Pituitary cancer, childhood: Cancer (malignant) of the pituitary gland in children. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the exact location of the tumor. Some pituitary tumors do not affect hormone production (nonfunctioning tumors).
• Pituitary tumors, adult: A benign or cancer tumor that develops in the tissue of the pituitary gland in adults. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the exact location of the tumor. Some pituitary tumors do not affect hormone production (nonfunctioning tumors).
• Placenta previa: Misplaced placenta covering the cervix
• Placental-site gestational trophoblastic tumor: A rare condition where cancer develops in the uterine muscle and in the site that the placenta was attached. The tumor forms after ectopic pregnancies, abortions or even following a normal delivery.
• Polycystic ovarian disease, familial: A rare familial condition characterized by menstrual abnormalities, excessive growth of hair, obesity and infertility.
• Polycystic ovaries urethral sphincter dysfunction: A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve.
• Polycystic ovary syndrome: Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects approximately 5% of all women.
• Polyembryoma: An aggressive type of tumor that develops from germ cells. It occurs mainly in the ovaries but sometimes in the testes.
• Prader-Willi syndrome: A rare genetic disorder characterized by reduced muscle tone, obesity and small hands and feet.
• Pregnancy symptoms: Symptoms related to pregnancy.
• Premenstrual syndrome: A collection of symptoms that some women suffer that occurs directly before menstruation
• Primary Fallopian Tube Cancer: A cancer that originates in the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon.
• Primary cortisol resistance: A rare genetic disorder where the body is unable to respond to a hormone called cortisol. The body produces excess cortisol to compensate for this defect.
• Primary hypothyroidism: Primary hypothyroidism is a condition in which a defect in the thyroid gland leads to reduced production of thyroid hormone.
• Primary malignant melanoma of the cervix: A form of cervical cancer where the tumor consists of pigment containing cells.
• Progeria short stature pigmented nevi: A very rare inherited disorder characterized by premature aging, short stature, and immune system deficiency. The type and severity of symptoms is variable.
• Prolactinoma: Benign cancer of the pituitary gland producing prolactin.
• Prolactinoma, familial: A pituitary tumor that secretes prolactin and occurs in a familial pattern of inheritance. The tumor is benign but can cause symptoms due to high prolactin levels or compression of the optic nerve.
• Pruritus Vulvae: Itching of the external genitalia of females.
• Pseudohermaphrodism - anorectal anomalies: A very rare disorder characterized by ambiguous external genitals and anal and rectal anomalies.
• Pseudohermaphroditism, female - skeletal anomalies: A rare disorder characterized by skeletal anomalies and ambiguous female genitals with female gonads.
• Psoriasis: Chronic skin rash condition, usually red or silver and blistery.
• Psychiatric disorders associated Celiac Disease: Patients with Psychiatric disorders are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Puerperal fever: Delayed uterine infection after childbirth
• Rectocele: Rectal prolapse with protrusion into the vagina
• Reduced menstrual flow: A reduced amount of blood loss during female menstruation
• Refractory Celiac Disease: Refractory Celiac Disease is celiac disease that fails to respond to treatment which involves a gluten-free diet. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The condition is quite uncommon and often the resulting poor absorption of nutrients from the intestines leads to a poor prognosis.
• Reiter’s syndrome: A form of reactive arthritis characterized by arthritis, urethritis, conjunctivitis and skin lesions.
• Renal nutcracker syndrome: A rare condition where the left renal vein becomes compressed between the abdominal aorta and the superior mesenteric artery. Symptoms usually don't become obvious until the third or fourth decade. The severity of the disorder is variable.
• Renoanogenital syndrome: A rare genetic disorder characterized by kidney, anal and genital abnormalities.
• Reproductive toxicity - Xylene (mixed isomers): Xylene (mixed isomers) is a suspected reproductive toxicant and exposure to it has the potential to negatively affect the human reproductive system. Xylene (mixed isomers) is used mainly as an industrial solvent and is used in the manufacture paints, lacquers, resins, inks and also in the manufacture of dyes, plastics and pharmaceuticals. The severity and nature of the adverse effect is variable and can be influenced by factors such as sex, level of exposure and individual sensitivity to the chemical. Effects on the female reproductive systems can include such things as menstrual problems, altered sexual behavior, infertility, altered puberty onset, altered length of pregnancy, lactation problems, altered menopause onset and pregnancy outcome. Effects on the male reproductive system can include such things as altered sexual behavior, altered fertility and problems with sperm shape or count.
• Resistance to LH (luteinizing hormone): A genetic abnormality where the body is unable to respond to luteinizing hormone which affects ovarian and testicular function.
• Resistance to thyroid stimulating hormone: A very rare disorder where the body is unable to respond to thyroid stimulating hormone even though it is present in sufficient quantities. The problem lies in defective thyroid stimulating hormone receptors.
• Retinitis pigmentosa, deafness, mental retardation, hypogonadism: A rare genetic disorder characterized by mental retardation, reduced hormone production by the testes or ovaries, deafness and vision problems.
• Rhabdomyosarcoma, Botryoid type: A type of cancer that arises from rhabdomyoblasts which are immature muscle cells. The tumors can occur arise from muscle tissue almost anywhere in the body but in the Botryoid form, tends to hollow organs with a mucosal lining such as the bladder, uterus and vagina. Symptoms depend on size and location of the tumor.
• Rud Syndrome: A condition characterized by ichthyosis, epilepsy, short stature, hypogonadism and severe mental retardation.
• Sarcoma botryoides: An aggressive form of cancer that arises from embryonic muscle cells. The tumor resembles a bunch of grapes and tends to occur in the genitourinary tract. Common locations are the cervix, vagina and bladder and very rare cases can occur in the bile duct or the soft tissues of the head and neck. It occurs most often in female infants and young children. Symptoms will vary depending on the exact location of the tumor.
• Satoyoshi syndrome: A very rare syndrome characterized by alopecia, diarrhea, skeletal abnormalities and painful leg cramps caused by physical exercise or emotional stress.
• Schroeder syndrome 1: High blood pressure and reduced salt concentration in sweat associated with an overactive adrenal cortex which is involved with hormone production.
• Secondary Dysmenorrhea: Menstrual-like cramping (dysmenorrhea) from an underlying condition.
• Secondary Fallopian Tube Cancer: A cancer that originates in some other part of the body and metastasizes to the fallopian tubes which form part of the female reproductive organs. This type of cancer is relatively uncommon.
• Secondary amenorrhea: Refers to the cessation of menstrual cycles to occur once they have already started.
• Secondary hypothyroidism: Secondary hypothyroidism is a condition in which the activity of the thyroid gland is decreased, due to failure of the pituitary gland or hypothalamus
• Secondary syphilis: A condition which is characterized by fever, multiform skin eruptions, iritis, alopecia, mucous patches and severe pain in the head and joints
• Semen allergy: An allergic reaction to the semen of a sexual partner. The reaction may be localized or systemic.
• Septic abortion: An abortion associated with a uterine infection. The infection can occur during or just before or after an abortion. The infection can result from factors such as Chlamydia, IUD's or attempted abortion using infected tools.
• Sertoli-leydig cell tumors: A rare form of ovarian cancer where excessive male sex hormones are produced by the cancerous cells.
• Sexual symptoms: Symptoms affecting the sexual organs
• Sexually Transmitted Diseases: Various diseases spread by sexual contact.
• Sheehan Syndrome: A rare condition that occurs in women who suffer a severe uterine hemorrhage during childbirth. The resulting blood loss may damage the pituitary gland and result in hypopituitarism.
• Sjogren's Syndrome: Autoimmune disease damaging the eye tear ducts and other glands.
• Sjogren's syndrome, juvenile, secondary to autoimmune disease: An autoimmune disorder that affects the glands involved in tear and saliva production as well as gastrointestinal tract moisture. It can occur as a secondary condition associated with other autoimmune disorders such as systemic lupus and rheumatoid arthritis.
• Sjögren syndrome, primary: An autoimmune disease where the body's immune system attacks parts of the body that produce moisture such as the eyes, mouth and gastrointestinal tract. Sjögren syndrome can occur on its own (primary) or with another connective tissue disease (secondary) such as rheumatoid arthritis, systemic lupus, systemic sclerosis and polymyositis/dermatomyositis. The condition can be mild or severe.
• Sjögren syndrome, secondary: An autoimmune disease where the body's immune system attacks parts of the body that produce moisture such as the eyes, mouth and gastrointestinal tract. Sjögren syndrome can occur on its own (primary) or with another connective tissue disease (secondary) such as rheumatoid arthritis, systemic lupus, systemic sclerosis and polymyositis/dermatomyositis. The condition can be mild or severe.
• Smoking: The smoking of cigarettes
• Sore vagina:
• Spotting: Mild vaginal bleeding
• Staphylococcal toxic shock syndrome: A very rare, potentially fatal infection caused by the bacterial toxins produced by Staphylococcus aureus or Streptococcus pyogenes. The condition is often associated with tampon use but can originate from other sources.
• Streptococcal Group B invasive disease: Infection with bacteria called Group B Streptococcus which can cause severe symptoms or even death. The bacteria occur in the stomach and the urogenital tract of females and are normally harmless and cause no symptoms. However, it can cause a range of diseases in newborns, the elderly and people with poor immune systems.
• Stress incontinence: The occurrence of incontinence when the bladder is under stress
• Stuart factor deficiency, acquired: A rare blood clotting disorder which causes mild to severe bleeding depending on the degree of deficiency of Factor X (Stuart factor). This disorder can be inherited or acquired by people suffering from conditions such as liver disease, amyloidosis, certain cancers and leprosy.
• Stuart factor deficiency, congenital: A rare inherited blood clotting disorder which causes mild to severe bleeding depending on the degree of deficiency of Factor X (Stuart factor).
• Substance abuse: Abuse of illicit substances
• Susceptibility to Celiac Disease 1: Susceptibility to celiac disease 1 is a term allocated to a genetic defect on a particular chromosome (chromosome 6p21.3) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 10: Susceptibility to celiac disease 10 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q25-q26) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 11: Susceptibility to celiac disease 11 is a term allocated to a genetic defect on a particular chromosome (chromosome 3q28) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 12: Susceptibility to celiac disease 12 is a term allocated to a genetic defect on a particular chromosome (chromosome 6q25) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 13: Susceptibility to celiac disease 13 is a term allocated to a genetic defect on a particular chromosome (chromosome 12q24) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 2: Susceptibility to celiac disease 2 is a term allocated to a genetic defect on a particular chromosome (chromosome 5q31-q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 3: Susceptibility to celiac disease 3 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q33) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 4: Susceptibility to celiac disease 4 is a term allocated to a genetic defect on a particular chromosome (chromosome 19p13.1) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 5: Susceptibility to celiac disease 5 is a term allocated to a genetic defect on a particular chromosome (chromosome 15q11-q13) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 6: Susceptibility to celiac disease 6 is a term allocated to a genetic defect on a particular chromosome (chromosome 4q27) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 7: Susceptibility to celiac disease 7 is a term allocated to a genetic defect on a particular chromosome (chromosome 1q133) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 8: Susceptibility to celiac disease 8 is a term allocated to a genetic defect on a particular chromosome (chromosome 2q11-q12) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Susceptibility to Celiac Disease 9: Susceptibility to celiac disease 9 is a term allocated to a genetic defect on a particular chromosome (chromosome 3p21) which makes a patient more susceptible to developing celiac disease. However, it is important to note that having the genetic anomaly does not mean a person will definitely develop celiac disease. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Syphilis: A sexually transmitted disease caused by a bacteria (Treponema pallidum). The condition is often asymptomatic in the early stages but one or more sores may be present in the early stages. Untreated syphilis usually results in remission of visible symptoms but further severe damage may occur to internal organs and other body tissues which can result in death.
• Tertiary hypothyroidism: Tertiary hypothyroidism results from a malfunction of the hypothalamus, the part of the brain that controls the endocrine system.
• Testicle disorders: Any condition that affects the testicles
• Tetrasomy X: A rare chromosomal disorder which causes mental retardation, small head and various other anomalies.
• Thrombasthenia: An inherited blood clotting disorder where abnormal blood platelet function causes results in excessive bleeding.
• Thrombocytopenia: Decreased concentration of platelets in the blood.
• Thrombocytopenic purpura, autoimmune: A rare blood disorder where a low number of platelets impairs the bloods ability to clot and results in bleeding into the skin and mucous membranes.
• Thyroid disorders: Any disorder of the thyroid gland.
• Thyroid hormone plasma membrane transport defect: Thyroid problems caused by a defect in the transport of a thyroid hormone called T4 (thyroxine) within the body. The thyroid produces excessive hormones to try to compensate for that inability of the body to utilize the hormone.
• Toe syndactyly, telecanthus, and anogenital and renal malformations: A rare X-linked syndrome characterized by webbed toes, telecanthus and kidney, genital and anal malformations.
• Torulopsis: A type of yeast infection caused by Torulopsis glabrata. The fungus is often found in normal healthy skin, respiratory system, genitourinary system and gastrointestinal system and it generally only becomes a problem in weakened or immunocompromised people. They type of symptoms are determined by where and how severe the infection is.
• Treponema infection: A rare infectious diseases which is transmitted through sexual contact and caused by Treponema pallidum (a spirochete bacterium). Untreated cases can result in severe complications and even death.
• Trichomoniasis: Sexually transmitted parasitic infection.
• Troell-Junet syndrome: A disorder involving enlarged extremities, diabetes, skull abnormalities and excessive thyroid hormone production.
• Trophoblastic Cancer: A neoplastic disorder that originates in the placenta
• Tubal ligation syndrome: A complication that can occur after sterilization using tubal ligation in females.
• Turner syndrome associated Celiac Disease: Females with Turner syndrome are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Type 1 diabetes related Celiac Disease: Patients with Type 1 diabetes are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• Urethral cancer: A rare cancer that develops in the urethra which carries urine from the bladder to be excreted.
• Urinary incontinence: Inability to fully control urination.
• Uterine Cancer: Cancer of the uterus.
• Uterine fibroids: Benign nodules in the uterus wall.
• Uterine prolapse: Prolapse of the uterus into the wrong position
• Uterine sarcoma: A rare type of cancer that occurs in the uterus or associated tissues. A sarcoma is a cancer that involves soft tissue and connective tissue such as bone, cartilage, fat, muscle and blood vessels.
• Uterus conditions: Any condition that affects the female uterus
• Uterus symptoms: Symptoms affecting the female uterus
• Vagina cancer: Cancer of the vagina.
• Vagina conditions: Any condition that affects the female vagina
• Vaginal bleed in pregnancy: Vaginal bleed in pregnancy refers to blood often found on underwear, the toilet paper, in the toilet bowl or after sexual intercourse. The blood loss may or may not be accompanied by other symptoms such as pain.
• Vaginal bleeding: Bleeding in or from the vagina.
• Vaginal bleeding after menopause: Any bleeding which occurs from the vagina after menopause
• Vaginal bulge: Bulge or protrusion inside the vagina
• Vaginal burning sensation: A burning sensation located in the vagina
• Vaginal candidiasis: Fungal infection of the vagina, sometimes called thrush.
• Vaginal discharge: Discharge from the vagina as a symptom
• Vaginal dryness: Lack of adequate vaginal lubrication.
• Vaginal fistula: Fistula between vagina and another cavity
• Vaginal irritation: Any irritation which occurs in the vagina
• Vaginal itching: Itching inside the vagina
• Vaginal odor: Vaginal smell or scent symptoms
• Vaginal pain: Pain affecting the vagina
• Vaginal paresthesia/ tingling: A loss of sensation located at or around the vagina
• Vaginal rash: An eruption on the skin of the vagina.
• Vaginal swelling: Swelling of the vagina.
• Vaginal symptoms: Symptoms related to the vagina
• Vaginitis: A condition which is characterized by inflammation to the vagina
• Virilising ovarian tumour: A tumour that results in the virilization of females due to hormone release
• Virilism: Masculinization - enhancement of male secondary sexual characteristics in females such as increased hair growth, deeper voice and baldness.
• Virilizing ovarian tumor: An ovarian tumor made up of hormone secreting cells which results in excessive male hormone (androgen) production.
• Vitamin A embryopathy: A morbid condition of the embryo caused by the consumption of excess Vitamin A during pregnancy
• Vitamin A overdose: Overdose of Vitamin A usually due to Vitamin A supplement overuse or poisoning.
• Vohwinkel syndrome: A rare condition where tight bands of thickened skin form around the base of fingers and toes and generally leads to self-amputation of the digit. Hearing loss is also associated with the condition.
• Von Willebrand disease: A rare inherited blood coagulation disorder characterized by a deficiency or defect in plasma protein called the von Willebrand factor which leads to bleeding problems
• Von Willebrand disease, dominant form: A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time.
• Von Willebrand disease, platelet type: A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time.
• Von Willebrand disease, recessive form: A condition that is characterised by autosomal inheritance and is a disorder that is charaterised by prolonged bleeding time.
• Von Willebrand disease, type 1: A rare inherited blood coagulation disorder characterized by a deficiency in plasma protein called the von Willebrand factor which leads to bleeding problems. Most cases of von Willebrand disease are type 1 which is the mildest form of the condition. Patients rarely have severe bleeding problems but may bleed excessively during surgery, dental work or due to a traumatic injury.
• Von Willebrand disease, type 2: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 is further subdivided into 4 subtypes, each with a different underlying genetic defect. The different subtypes have different methods of treatment so an correct diagnosis is important. The severity of the bleeding symptoms is variable.
• Von Willebrand disease, type 2A: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. The severity of the bleeding symptoms is variable.
• Von Willebrand disease, type 2B: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. The severity of the bleeding symptoms is variable. Type 2B often requires a different medication to the other subtypes.
• Von Willebrand disease, type 2M: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. Type 2M is very rare. The severity of the bleeding symptoms is variable.
• Von Willebrand disease, type 2N: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. The severity of the bleeding symptoms is variable.
• Von Willebrand disease, type 3: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 3 is the most severe form of von Willebrand Disease.
• Vulva bruise: A haematoma that occurs on the vulva.
• Vulva burning sensation: A burning sensation located on the vulva
• Vulva itch: Itching of the vulva area
• Vulva paresthesia/ tingling: A loss of sensation located at or around the vulva.
• Vulva rash: An eruption on the skin of the vulva.
• Vulva swelling: A swelling located on the vulva.
• Vulva symptoms: Symptoms related to the vulva (external skin region near vagina)
• Vulva tingling/ paresthesias: A tingling and numbness located in the vulva
• Vulval Ulceration: an area of tissue erosion in the vulva
• Vulval swelling: Swelling of the external female genitalia.
• Vulvar Diseases: Any disease that involves the vulva which is a part of the female genitalia. Diseases can include cancer or fungal, bacterial or viral infections. Symptoms and prognosis will vary depending on the disease process involved.
• Vulvar lesion: A condition which is characterized by lesion located on the vulvar
• Vulvar neoplasms: A tumor that develops in the tissue of the vulva.
• Vulvar vestibulitis syndrome: The inflammation of the opening of the vagina.
• Vulvitis: Any inflammation which occurs to the vulva
• Vulvovaginitis: A condition which is characterized by inflammation to the vular and vagina
• WHIM syndrome: A rare syndrome characterized by warts, hypogammaglobulinemia (low blood gammaglobulin levels), recurring bacterial infections and myelokathexis (form of neutropenia). It is a form of immunodeficiency disease caused by a mutation in a chemokine receptor.
• Wandering spleen: A very rare birth defect where the structures (ligaments) that hold the spleen in position are absent or not developed properly which allows the spleen to move around in the abdominal cavity.
• Werner syndrome: A form of premature aging where sufferers start aging during adolescence or soon after and appear old by the time they reach their 30's or 40's. Milder forms of the condition may also occur.
• Willebrand disease, acquired: A bleeding disorder characterised by prolonger bleeding time
• William's syndrome associated Celiac Disease: Patients with William's syndrome are more susceptible to developing celiac disease than the average population. Celiac disease is an autoimmune disorder characterized by intolerance to gluten by the small intestine. The type and severity of symptoms varies amongst people - some people have severe gastrointestinal symptoms from infancy whereas other have no symptoms other than fatigue or anemia during adulthood.
• XK aprosencephaly: An extremely rare condition where the forebrain is absent as well as other abnormalities.
• XX male syndrome: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
• XY female: A person who has a chromosome composition of 46 XY and who is phenotypically female
• Y chromosome pericentric inversion: A genetic abnormality that usually results in the miscarriage of a fetus
• Yellow vaginal discharge: purulent vaginal discharge
• Yolk sack tumour: A germ cell tumour that is a proliferation of yolk sack endoderm
• Yusho disease: A condition that affects the menstrual cycle of female as well as having effects on the immune system
• Zadik Barak Levin syndrome: A condition that affects the endocrine system as well as some facial characteristics

 » Next page: Surveys

Rate This Website

What do you think about the features of this website? Take our user survey and have your say:

Website User Survey

Medical Tools & Articles:

Next articles:

• Surveys
• Join in at the forums

Tools & Services:

• Bookmark this page
• Surveys relating to Female sexual symptoms
• Symptom Search
• Symptom Checker
• Medical Dictionary
• Give your feedback

Medical Articles:

• Disease & Treatments Search
• Misdiagnosis Center
• Full list of interesting articles

Forums & Message Boards

• Ask or answer a question at the Boards:
• I cannot get a diagnosis. Please help.
• Tell us your medical story.
• Share your misdiagnosis story.
• What is the best treatment for my condition?
• See all the Boards.

Enter your search terms Submit search form
Search The Web Search wrongdiagnosis.com

Common Health Mistakes

Symptom
Checker

Search Specialists by State and City