Causes of Short stature - hyperkaliemia - acidosis

Short stature - hyperkaliemia - acidosis as a complication of other conditions:

Other conditions that might have Short stature - hyperkaliemia - acidosis as a complication may, potentially, be an underlying cause of Short stature - hyperkaliemia - acidosis. Our database lists the following as having Short stature - hyperkaliemia - acidosis as a complication of that condition:

• Autoimmune thyroid disease associated Celiac Disease
• Bamboo hair syndrome
• Celiac Disease
• Collagenous celiac disease
• Comel-Netherton Syndrome
• Down's syndrome associated Celiac Disease
• Failure To Thrive
• Gloomy syndrome
• Netherton syndrome ichthyosis
• Osteochondroma
• Psychiatric disorders associated Celiac Disease
• Refractory Celiac Disease
• Renal osteodystrophy
• Susceptibility to Celiac Disease 1
• Susceptibility to Celiac Disease 10
• Susceptibility to Celiac Disease 11
• Susceptibility to Celiac Disease 12
• Susceptibility to Celiac Disease 13
• Susceptibility to Celiac Disease 2
• Susceptibility to Celiac Disease 3
• Susceptibility to Celiac Disease 4
• Susceptibility to Celiac Disease 5
• Susceptibility to Celiac Disease 6
• Susceptibility to Celiac Disease 7
• Susceptibility to Celiac Disease 8
• Susceptibility to Celiac Disease 9
• Turner syndrome associated Celiac Disease
• Type 1 diabetes related Celiac Disease
• William's syndrome associated Celiac Disease

Short stature - hyperkaliemia - acidosis as a symptom:

Conditions listing Short stature - hyperkaliemia - acidosis as a symptom may also be potential underlying causes of Short stature - hyperkaliemia - acidosis. Our database lists the following as having Short stature - hyperkaliemia - acidosis as a symptom of that condition:

• 3C syndrome
• 49,XXXXX syndrome
• 49,XXXXY syndrome
• Aarskog Syndrome
• Abidi X-linked mental retardation syndrome
• Abruzzo Erickson syndrome
• Acanthocytosis
• Achalasia - addisonianism - alacrima syndrome
• Achalasia - Addisonianism - Alacrimia syndrome
• Achalasia - adrenal - alacrima syndrome
• Achondrogenesis, type 3
• Achondroplasia
• Acrocapitofemoral dysplasia
• Acrodysostosis
• Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia
• Acrofacial dysostosis Catania form
• Acrofacial dysostosis postaxial, atypical
• Acrofacial dysostosis Rodriguez type
• Acrofacial dysostosis, Palagonia type
• Acrofrontofacionasal dysostosis syndrome
• Acrogeria (Gottron Type)
• Acromesomelic dysplasia Brahimi Bacha type
• Acromesomelic dysplasia Campailla Martinelli type
• Acromesomelic dysplasia Hunter Thompson type
• Acromesomelic dysplasia, Maroteaux type
• Acromicric dysplasia
• Acroosteolysis dominant type
• Adrenal adenoma, familial
• Adrenal Cancer
• Adrenal Cortex Neoplasms
• Adrenal gland hyperfunction
• Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency
• Adrenal hypoplasia congenital, X-linked
• Adrenal incidentaloma
• Adrenocortical carcinoma
• Agenesis of the corpus callosum - mental retardation - coloboma - micrognathia
• Akaba-Hayasaka syndrome
• Akesson syndrome
• Al Awadi syndrome
• Al Awadi-Raas-Rothschild syndrome
• Al Gazali Aziz Salem syndrome
• Albright like syndrome
• Albright's hereditary osteodystrophy
• Alopecia mental retardation syndrome
• Alpha-ketoglutarate dehydrogenase deficiency
• Alves Castelo dos Santos syndrome
• Amish brittle hair syndrome
• Ampola syndrome
• Andersen-Tawil syndrome
• Angel shaped phalangoepiphyseal dysplasia
• Angiokeratoma - mental retardation - coarse face
• Aniridia - renal agenesis - psychomotor retardation
• Ankle defects short stature
• Anophthalmia - hypothalamo-pituitary insufficiency
• Anophthalmia - hypyothalamo-pituitary insufficiency
• Anophthalmia - short stature - obesity
• Apelt-Gerkin-Lenz Syndrome
• Aphalangia - syndactyly - microcephaly
• AREDYLD
• Arima syndrome
• Arthritis - short stature - deafness
• Arthrogryposis distal type II
• Arthrogryposis IUGR thoracic dystrophy
• Arthrogryposis multiplex congenita type 2B
• Arthrogryposis, distal, type 2B
• Arthrogryposis-like hand anomaly - sensorineural deafness
• Arthropathy, progressive pseudorheumatoid, of childhood
• Aspartylglucosaminidase deficiency
• Aspartylglucosaminuria
• Aspartylglycosaminuria
• Asymmetric short stature syndrome
• Ataxia - diabetes - goiter - gonadal insufficiency
• Atelosteogenesis, type 1
• Athabaskan severe combined immunodeficiency
• Atkin-Flatiz syndrome
• Atrichia - mental and growth delay
• Aural atresia - multiple congenital anomalies - mental retardation
• Axenfeld-Rieger syndrome
• Babinski-Froelich Syndrome
• Bagatelle-Cassidy syndrome
• Bangstad syndrome
• Bardet-Biedl Syndrome
• Bardet-Biedl syndrome, type 1
• Bardet-Biedl syndrome, type 10
• Bardet-Biedl syndrome, type 11
• Bardet-Biedl syndrome, type 12
• Bardet-Biedl syndrome, type 2
• Bardet-Biedl syndrome, type 3
• Bardet-Biedl syndrome, type 4
• Bardet-Biedl syndrome, type 5
• Bardet-Biedl syndrome, type 6
• Bardet-Biedl syndrome, type 7
• Bardet-Biedl syndrome, type 8
• Bardet-Biedl syndrome, type 9
• Barrow-Fitzsimmons Syndrome
• Bartter Syndrome
• Bartter's syndrome, antenatal type 1
• Bartters syndrome, antenatal , type 2
• Bellini-Chiumello-Rinoldi syndrome
• Berk-Tabatznik syndrome
• Berlin Breakage syndrome
• Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification
• Bessel-Hagen disease
• BIDS syndrome
• Bindewald-Ulmer-Muller syndrome
• Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency
• Blepharo facio skeletal syndrome
• Blepharophimosis with ptosis, syndactyly, and short stature
• Blepharoptosis - aortic anomaly
• Blethen-Wenick-Hawkins syndrome
• Blomstrand syndrome
• Bloom Syndrome
• BOD syndrome
• Bone dysplasia, lethal, Holmgren type
• Bonneman-Meinecke-Reich syndrome
• Bonnemann-Meinecke-Reich syndrome
• Borrone-Di Rocco-Crovato syndrome
• Boudhina-Yedes-Khiari syndrome
• Bowing, congenital, short bones
• Boyd-Stearns syndrome
• Brachydactylous dwarfism, Mseleni type
• Brachydactyly - arterial hypertension
• Brachydactyly - mesomelia - mental retardation - heart defects
• Brachydactyly - small stature - face anomalies
• Brachydactyly - tibial hypoplasia
• Brachyolmia
• Branchial arch syndrome X-linked
• Brittle hair - mental deficiency
• Brosnan Syndrome
• Bullous dystrophy, macular type
• Buntinx-Lormans-Martin syndrome
• Camera-Marugo-Cohen syndrome
• Camptodactyly - joint contractures and facial skeletal dysplasia
• Camptodactyly syndrome, Guadalajara type 1
• Camptodactyly syndrome, Guadalajara type 2
• Camptodactyly syndrome, Guadalajara type 3
• Camptomelic syndrome
• Cantu syndrome
• Cardiocranial syndrome
• Cardiomelic syndrome Stratton Koehler type
• Cartilage-hair hypoplasia-like syndrome
• Cat Eye Syndrome
• Cataract - aberrant oral frenula - growth delay
• Cataract - ataxia - deafness
• Cataract deafness hypogonadism
• Caudal appendage - deafness
• CCFDN
• CDG syndrome type 1A
• Cerebellar hypoplasia - endosteal sclerosis
• Cerebro oculo skeleto renal syndrome
• Cerebrorenodigital syndrome
• Cerebrorenodigital syndrome with limb malformations and triradiate acetabula
• Childhood hypophosphatasia
• Chitty Hall Baraitser syndrome
• Cholestasis, progressive familial intrahepatic 2
• Cholestasis, progressive familial intrahepatic 3
• Chondrodysplasia punctata lethal neonatal
• Chondrodysplasia punctata with steroid sulfatase deficiency
• Chondrodysplasia punctata, humero-metacarpal type
• Chondrodysplasia, acromesomelic, with genital anomalies
• Chondrodysplasia, type Nance-Sweeney
• Chondroectodermal dysplasia
• Choroideremia - hypopituitarism
• Christian-Demyer-Franken syndrome
• Chromosome 1 ring
• Chromosome 1, 1p36 deletion syndrome
• Chromosome 1, deletion q21 q25
• Chromosome 1, duplication 1p21 p32
• Chromosome 1, monosomy 1p22 p13
• Chromosome 1, monosomy 1q25 q32
• Chromosome 1, monosomy 1q32 q42
• Chromosome 1, monosomy 1q4
• Chromosome 1, q42 11 q42 12 duplication
• Chromosome 1, trisomy 1q42 qter
• Chromosome 10p terminal deletion syndrome
• Chromosome 13p duplication
• Chromosome 14 deletion
• Chromosome 14q, proximal duplication
• Chromosome 14q, terminal duplication
• Chromosome 15q26-qter Deletion Syndrome
• Chromosome 17 deletion
• Chromosome 17 trisomy
• Chromosome 17, trisomy 17p11.2
• Chromosome 17p, partial deletion
• Chromosome 18q, partial deletion
• Chromosome 2, monosomy 2pter p24
• Chromosome 2, monosomy 2q37
• Chromosome 21, monosomy 21q22
• Chromosome 22, microdeletion 22q11
• Chromosome 22q11 deletion
• Chromosome 3, monosomy 3p25
• Chromosome 3, trisomy 3q13 2 q25
• Chromosome 4, Monosomy Distal 4q
• Chromosome 4, trisomy 4p
• Chromosome 7, monosomy 7q21
• Chromosome 7, monosomy 7q3
• Chromosome 7, trisomy 7p13 p12 2
• Chromosome 7, trisomy mosaic
• Chromosome 9, Trisomy 9p (Multiple Variants)
• Chromosome 9, trisomy 9q32
• Chudley syndrome 1
• Chylomicron retention disease with Marinesco-Sjogren syndrome
• Citrulline transport defect
• Clavicle, pseudoarthrosis of, congenital
• Cleft palate - coloboma - deafness
• Cleft palate - short stature - vertebral anomalies
• Cleidocranial dysplasia
• Cleidorhizomelic syndrome
• Coarse face - hypotonia - constipation
• Cockayne syndrome type 1
• Cockayne syndrome type 2
• Cockayne syndrome type 3
• Coffin syndrome 1
• Coffin-Lowry syndrome
• Collagenopathy, type 2 alpha 1
• Collins-Dennis-Clarke-Pope Syndrome
• Complex 2 mitochondrial respiratory chain deficiency
• Congenital disorder of glycosylation type 1A
• Congenital disorder of glycosylation type 2C
• Congenital disorder of glycosylation type X - Bombay blood group phenotype
• Congenital Disorders of Glycosylation Type Ia
• Congenital fiber type disproportion
• Congenital heart disease - radio ulnar synostosis - mental retardation
• Copper deficiency, familial benign
• Cormier Rustin Munnich syndrome
• Corneal anesthesia deafness intellectual deficit
• Corneal anesthesia deafness mental retardation
• Corneal hypesthesia deafness intellectual deficit
• Cornelia de Lange syndrome 1
• Corneodermatoosseous syndrome
• Cortical blindness - mental retardation - polydactyly
• Coxoauricular syndrome
• Crandall syndrome
• Cranio-facio-cardio-skeletal dysplasia
• Cranioacrofacial syndrome
• Craniodigital syndrome - mental retardation
• Craniofacial dysostosis - arthrogryposis - progeroid appearence
• Craniofacial dyssynostosis
• Craniofaciocardioskeletal syndrome
• Craniofrontonasal dysplasia
• Craniostenosis with congenital heart disease mental retardation
• Craniosynostosis - alopecia - brain defect
• Craniosynostosis - congenital heart disease - mental retardation
• Craniosynostosis - intracranial calcifications
• Creatine deficiency, X-linked
• Culler-Jones syndrome
• D ercole syndrome
• Daentl-Townsend-Siegel syndrome
• Daentl-Towsend-Siegel syndrome
• Dahlberg syndrome
• Dauwerse-Peters syndrome
• Davis-Lafer syndrome
• De Barsy Syndrome
• De Hauwere Leroy Adriaenssens syndrome
• Deafness - cataracts - skeletal anomalies
• Deafness - epiphyseal dysplasia - short stature
• Deafness neurosensory - pituitary dwarfism
• Deafness symphalangism
• Deafness-mental retardation, Martin-Probst type
• Del (2) (q24.3-q31)
• Del (2) (q33-q36)
• Del (2) (q34-q36)
• Del (2) (q35-qter)
• Del (2) (q36-qter)
• Del (2) (q37.3-qter) and dup (8) (q24.3-qter))
• Del (3) (p21.1-p13)
• Del (3) (q12-q21)
• Del(1) (pter-p34)
• Del(1) (q44-qter)
• Deletion 10pter
• Deletion 10q
• Deletion 11q
• Deletion 5p
• Dennis cohen syndrome
• Dentinogenesis imperfecta - short stature - hearing loss - mental retardation
• Desbuquois dysplasia-like syndrome
• Devriendt syndrome
• Diabetes insipidus, nephrogenic type 2
• Diabetes insipidus, nephrogenic, dominant type
• Diabetes insipidus, nephrogenic, recessive type
• Diaphyseal aclasis
• Diastrophic dysplasia
• Dibasic aminoaciduria 2
• DiGeorge syndrome
• Distal arthrogryposis, Moore-Weaver type
• Distinctive Craniofacial Features - Pterygia - Mental Retardation
• Dobrow syndrome
• Dup (1) (q11-q22)
• Dup (2) (pter-p23)
• Dup (2) (q11.2-q14.2)
• Dup (2) (q11.2-q21.1)
• Dup (3) (pter-p25)
• Dup(1) (p31-p21)
• Dup(1) (p32-p21.2)
• Dup(1) (q24-q41)
• Dwarfism
• Dwarfism - bluish sclerae
• Dwarfism - stiff joint - ocular abnormalities
• Dwarfism - tall vertebrae
• Dwarfism - thin bones - multiple fractures
• Dyggve-Melchior-Clausen Syndrome
• Dyschondrosteosis - nephritis
• Dysequilibrium syndrome
• Dysmorphism - abnormal vocalization - mental retardation
• Dysosteosclerosis
• Dysostosis
• Dysostosis acral with facial and genital abnormalities
• Dysplastic cortical hyperostosis
• Dyssegmental dysplasia
• Ear, patella, short stature syndrome
• Ectodermal dysplasia - arthrogryposis - diabetes mellitus
• Ectodermal dysplasia - blindness
• Ectodermal dysplasia - hypohidrotic - hypothyroidism - ciliary diskinesia
• Ectodermal dysplasia - neurosensory deafness
• Ectodermal dysplasia with natal teeth, Turnpenny type
• Ectodermal dysplasia, Berlin type
• Ehlers-Danlos syndrome, classic type
• Ehlers-Danlos syndrome, progeroid form
• Ehlers-Danlos syndrome, progeroid form 2
• Empty Sella Syndrome
• Encephalopathy - intracranial calcification - growth hormone deficiency - microcephaly - retinal degeneration
• Enchondromatosis-dwarfism-deafness
• Eng Strom syndrome
• Engelhard-Yatziv syndrome
• Epidermal nevus - vitamin D resistant rickets
• Epilepsy - telangiectasia
• Epimetaphyseal skeletal dysplasia
• Epiphyseal dysplasia - hearing loss - dysmorphism
• Epiphyseal dysplasia dysmorphism camptodactyly
• Epiphyseal dysplasia, multiple
• Epiphyseal dysplasia, multiple, 1
• Epiphyseal stippling syndrome - osteoclastic hyperplasia
• Escobar syndrome, type B
• Exostoses, multiple
• Exostoses, multiple, type 1
• Extrasystoles - short stature - hyperpigmentation - microcephaly
• Eye defects - arachnodactyly - cardiopathy
• FACES syndrome
• Facio-auriculo-radial dysplasia
• Faciodigitogenital syndrome, recessive form
• Fanconi pancytopenia
• Fara-Chlupackova syndrome
• Faye-Petersen-Ward-Carey syndrome
• Femur-fibula-ulna syndrome
• Fenton-Wilkinson-Toselano syndrome
• Fernhoff-Blackston-Oakley syndrome
• Fetal methylmercury syndrome
• FG Syndrome
• FG syndrome 1
• FG syndrome 2
• FG syndrome 3
• FG syndrome 4
• FG syndrome 5
• Fibrochondrogenesis
• Fibula aplasia complex - brachydactyly
• Filippi Syndrome
• Fitzsimmons-Guilbert syndrome
• Fitzsimmons-Walson-Mellor syndrome
• Fleisher syndrome
• Forbes disease
• Forney Robinson Pascoe syndrome
• Frank-Ter Haar syndrome
• Fraser-Jequier-Chen syndrome
• Frias syndrome
• Froelich's syndrome
• Frolich's syndrome
• Froster-Iskenius-Waterson syndrome
• Fryns-Smeets-Thiry syndrome
• Frölich's syndrome
• Functioning pancreatic endocrine tumor
• Gangliosidosis, generalized GM1 type 3
• Garret-Tripp syndrome
• Gay-Feinmesser-Cohen syndrome
• Geleophysic dwarfism
• GEMSS syndrome
• Generalized lipodystrophy with mental retardation, deafness, short stature and slender bones
• Geroderma osteodysplastica
• Gerodermia osteodysplastica
• Gerodermia osteodysplastica hereditaria
• Gerodermia osteodysplasticum
• Gitelman syndrome
• Glaucoma ectopia microspherophakia stiff joints short stature
• Glomerulonephritis - sparse hair - telangiectases
• Glycogen branching deficiency
• Glycogen debranching deficiency
• Gms syndrome
• Goldberg-Shprintzen megacolon syndrome
• Gollop syndrome
• Gomez and Lopez-Hernandez syndrome
• Gonadal dysgenesis XY type associated anomalies
• Gracile bone dysplasia
• Grant syndrome
• Greenberg dysplasia
• Grix-Blankenship-Peterson syndrome
• Growth deficiency brachydactyly unusual facies
• Growth delay due to insulin-like growth factor I resistance
• Growth Hormone Deficiency
• Growth Hormone Receptor Deficiency
• Guizar-Vasquez-Luengas syndrome
• Guizar-Vasquez-Sanchez-Manzano syndrome
• Gurrieri-Sammito-Bellussi syndrome
• Harper dwarfism
• Haspeslagh Fryns Muelenaere syndrome
• Heart defects - limb shortening
• Herrmann Opitz arthrogryposis syndrome
• Herrmann-Opitz craniosynostosi
• Howard-Young syndrome
• Hoyeraal-Hreidarsson syndrome
• Humerospinal dysostosis - congenital heart disease
• Hunter-Carpenter-Macdonald syndrome
• Hunter-MacDonald syndrome
• Hunter-McAlpine syndrome
• Hunter-Mcdonald syndrome
• Hutterite cerebroosteonephrodysplasia syndrome
• Hydrocephalus obesity hypogonadism
• Hyperadrenalism
• Hyperparathyroidism, neonatal severe primary
• Hypogonadism
• Hypogonadism - mitral valve prolapse - mental retardation
• Hypogonadism hypogonadotropic due to mutations in GR hormone
• Hypogonadotropic hypogonadism - syndactyly
• Hypomelanosis of Ito
• Hypoparathyroidism - short stature - mental retardation
• Hypoparathyroidism familial isolated
• Hypoparathyroidism X-linked
• Hypophosphatemia, Familial
• Hypophosphatemic rickets
• Hypopituitarism postaxial polydactyly
• Hypopituitary dwarfism
• Hypotelorism - cleft palate - hypospadias
• Hypothyroidism - dermoid cyst - cleft palate
• IBIDS syndrome
• ICF syndrome
• Ichthyosis and male hypogonadism
• Ichthyosis male hypogonadism
• Immunodeficiency due to defect in MAPBP-interacting protein
• Incontinentia Pigmenti
• Intellectual deficit - cataracts - calcified pinnae - myopathy
• Intellectual deficit - multiple anomalies
• Intellectual deficit - short stature - microcephaly - eye anomalies
• Iris dysplasia hypertelorism deafness
• Iris dysplasia with ocular hypertelorism, psychomotor retardation and sensorineural deafness
• Ischiadic hypoplasia - renal dysfunction - immunodeficiency
• Jacobsen syndrome
• Jeune syndrome
• Jorgenson-Lenz syndrome
• Juberg-Hayward syndrome
• Juberg-Marsidi syndrome
• Juvenile macular degeneration and hypotrichosis
• Juvenile macular degeneration, hypotrichosis
• Juvenile Paget disease
• Kantaputra-Gorlin syndrome
• Kaplan-Plauchu-Fitch syndrome
• Kaplowitz-Bodurtha syndrome
• Kashani-Strom-Utley syndrome
• KBG Syndrome
• Kearns-Sayre Syndrome
• Kennerknecht syndrome
• Kennerknecht-Vogel syndrome
• Keratosis follicularis - dwarfism - cerebral atrophy
• King-Denborough syndrome
• Klippel Feil deformity conductive deafness absent vagina
• Kniest dysplasia
• Koussef nichols syndrome
• Kousseff-Nichols syndrome
• Kozlowski-Celermajer syndrome
• Laron Dwarfism
• Laron Pituitary Dwarfism
• Laron Syndrome
• Laron syndrome type 1
• Laron syndrome type 2
• Laron Type Pituitary Dwarfism 1
• Laron-type dwarfism
• Laron-type Dwarfism Phenotypic Syndrome
• Larsen syndrome, dominant type
• Larsen-like syndrome, lethal form
• Larsen-like syndrome, lethal type
• Laryngeal web congenital heart disease short stature
• Larynx atresia
• Lateral meningocele syndrome
• Le Marec-Bracq-Picaud syndrome
• Lenz Majewski hyperostotic dwarfism
• Lenz Microphthalmia Syndrome
• Leri Pleonosteosis
• Lethal chondrodysplasia, Moerman type
• Limb transversal defect - cardiac anomaly
• Lindstrom syndrome
• Localized epiphyseal dysplasia
• Lockwood-Feingold syndrome
• Long thumb brachydactyly, maxillary hypoplasia, mental retardation and unusual facies
• Lowry-Wood syndrome
• Lumbar malsegmentation - short stature
• Lumbar malsegmentation, short stature and facial anomalies
• Lymphedema, congenital
• Macrocephaly - short stature - paraplegia
• Macrocephaly, mental retardation, short stature, spastic paraplegia and CNS malformations
• Macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance
• Macules hereditary congenital hypopigmented hyperpigmented
• Macules, hereditary, congenital hypopigmented and hyperpigmented
• Majeed syndrome
• Malocclusion - short stature syndrome
• Mandibuloacral dysplasia
• Mandibuloacral dysplasia with type A lipodystrophy
• Mandibuloacral dysplasia with type B lipodystrophy
• Marinesco-Sjogren syndrome
• Marinesco-Sjögren I
• Maroteaux-Stanescu-Cousin syndrome
• Marshall syndrome
• Martsolf syndrome
• Mastocytosis - short stature - hearing loss
• Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia
• Matsoukas-Liarikos-Giannika syndrome
• Mayer-Rokitansky-Kuster-Hauser, syndrome, type 2 (MRKH type 2)
• McDonough syndrome
• McKusick type metaphyseal chondrodysplasia
• Medrano-Roldan syndrome
• Megarbane syndrome
• Megarbane-Loiselet syndrome
• Meier-Rotschild syndrome
• MELAS
• Mental mixed retardation - deafness - clubbed digits
• Mental mixed retardation deafnes clubbed digits
• Mental retardation - hip luxation - G6PD variant
• Mental retardation - hypotonic facies syndrome, X-linked, 1
• Mental retardation - macrocephaly - coarse facies - hypotonia
• Mental retardation - microcephaly - phalangeal - facial abnormalities
• Mental retardation - myopathy - short stature - endocrine defect
• Mental Retardation - Pterygia - Shortness - Distinctive Facial Appearance
• Mental retardation - short stature - absent phalanges
• Mental retardation - short stature - cleft palate - unusual facies
• Mental retardation - short stature - deafness - genital
• Mental retardation - short stature - hand contractures - genital anomalies
• Mental retardation - short stature - heart and skeletal anomalies
• Mental retardation - short stature - microcephaly - eye anomalies
• Mental retardation - short stature - scoliosis
• Mental retardation - short stature - unusual facies
• Mental retardation - short stature, Bombay phenotype
• Mental retardation cataracts calcified pinnae myopathy
• Mental retardation unusual facies ampola type
• Mental retardation X-linked - psychosis - macroorchidism
• Mental retardation X-linked short stature obesity
• Mental retardation, Buenos Aires type
• Mental retardation, macrocephaly, short stature and craniofacial dysmorphism
• Mental retardation, Mietens-Weber type
• Mental retardation, Smith-Fineman-Myers type
• Mental retardation, X-linked - hypogonadism - ichthyosis - obesity - short stature
• Mental retardation, X-linked with brachydactyly and macroglossia
• Mental retardation, X-linked, 2
• Mental retardation, X-linked, 45
• Mental retardation, X-linked, Armfield type
• Mental retardation, X-linked, Cabezas type
• Mental retardation, X-linked, Raynaud type
• Mental retardation, X-linked, Shrimpton type
• Mental retardation, X-linked, Stoll type
• Mental retardation, X-linked, syndromic, due to JARID1C mutation
• Mental retardation, X-linked, Vitale type
• Mental retardation, X-linked, with isolated growth hormone deficiency
• Mental retardation, X-linked, Wittwer type
• Mesomelia
• Mesomelia radial hypoplasia bifid thumb unusual facies
• Mesomelic dysplasia, Savarirayan type
• Metaphyseal acroscyphodysplasia
• Metaphyseal chondrodysplasia Schmid type
• Metaphyseal chondrodysplasia Spahr type
• Metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands
• Metaphyseal chondrodysplasia, recessive type
• Metaphyseal dysostosis mental retardation conductive deafness
• Metaphyseal dysplasia - maxillary hypoplasia - brachydactyly
• Metatrophic dysplasia
• Metatropic dwarfism
• Methylmalonic aciduria - microcephaly - cataract
• Micro syndrome
• Microbrachycephaly - ptosis - cleft lip
• Microcephalic osteodysplastic dysplasia, Saul-Wilson type
• Microcephalic osteodysplastic primordial dwarfism types 1 and 3
• Microcephaly - cervical spine fusion anomalies
• Microcephaly - deafness syndrome
• Microcephaly - hypergonadotropic hypogonadism - short stature
• Microcephaly - microphthalmos - blindness
• Microcephaly immunodeficiency lymphoreticuloma
• Microcephaly micropenis convulsions
• Microcephaly, autosomal dominant
• Microdontia - hypodontia - short stature
• Micromelic dysplasia - dislocation of radius
• Microphthalmia syndromic, type 9
• Microphthalmia, Lentz type
• Microphthalmia, syndromic 1
• Miescher syndrome (2)
• Miescher's syndrome
• Mietens syndrome
• Milner-Khallouf-Gibson syndrome
• Mitochondrial diseases, clinically indefinite
• Mitochondrial encephalomyopathy - aminoacidopathy
• Mitochondrial myopathy - lactic acidosis
• Mitochondrial neurogastrointestinal encephalopathy syndrome
• Monosomy 1p36
• Monosomy 8q21 q22
• Morava-Mehes syndrome
• Mowat-Wilson syndrome
• Moynahan syndrome III
• MRXS9
• Mucolipidosis III
• Mucopolysaccharidoses
• Mucopolysaccharidosis 1
• Mucopolysaccharidosis II
• Mucopolysaccharidosis type 6
• Mucopolysaccharidosis type 7 Sly syndrome
• Mucopolysaccharidosis, type 9
• Mulibrey Nanism syndrome
• Mullerian Aplasia - Renal Aplasia - Cervicothoracic Somite Dysplasia
• Multicentric osteolysis - nodulosis - arthropathy
• Multiple congenital anomalies - mental retardation - growth failure and cleft lip/ palate
• Multiple endocrine abnormalities - adenylyl cyclase dysfunction
• Multiple epiphyseal dysplasia
• Multiple Hereditary Exostoses
• Multiple joint dislocations - metaphyseal dysplasia
• Multiple pterygium syndrome
• Multiple pterygium syndrome, autosomal recessive
• MURCS Association
• Myoclonus with epilepsy with ragged red fibers
• Myopathy - growth and mental retardation - hypospadias
• Myopathy - growth delay - mental retardation - hypospadias
• Myopathy, congenital fiber-type disproportion
• Narrow oral fissure - short stature - cone-shaped epiphyses
• Navajo neurohepatopathy
• Nephrogenic diabetes insipidus
• Neuroaxonal dystrophy - renal tubular acidosis
• Neuroectodermal endocrine syndrome
• Neurofaciodigitorenal syndrome
• Neurofibromatosis syndrome
• Neurofibromatosis syndrome Type II
• Neurofibromatosis-2
• Neurofibromatosis-Noonan syndrome
• Nicolaides-Baraitser syndrome
• Nijmegen Breakage Syndrome
• Nodulosis-arthropathy-osteolysis syndrome
• Noonan Syndrome
• Noonan syndrome 3
• Noonan-like/multiple giant cell lesion syndrome
• Oculo skeletal renal syndrome
• Oculo tricho dysplasia
• Oculo-osteo-cutaneous syndrome
• Oculocerebral hypopigmentation syndrome, type Preus
• Oculomaxillofacial dysostosis
• Oculopalatocerebral syndrome
• Oculopalatoskeletal syndrome
• Oculorenocerebellar syndrome
• OFD syndrome type 8
• Oligodontia, microcephaly, short stature and characteristic facies
• Ollier Disease
• Omodysplasia
• Omodysplasia type 1
• Opsismodysplasia
• Oral facial digital syndrome, type 4
• Oral facial digital syndrome, type IV
• Oslam syndrome
• OSMED, Homozygous
• Ossified Ear cartilages with Mental deficiency, Muscle Wasting and Bony Changes
• Osteogenesis imperfecta congenita, microcephaly, and cataracts
• Osteogenesis imperfecta, type 5
• Osteogenesis imperfecta, type 6
• Osteogenesis imperfecta, type 7
• Osteopetrosis, mild autosomal recessive form
• Oto-facio-osseous-gonadal syndrome
• Oto-spondylo-megaepiphyseal dysplasia, autosomal recessive
• Oto-spondylo-megaepiphyseal dysplasia, homozygous
• Otopalatodigital Syndrome Type I and II
• Otospondylomegaepiphyseal dysplasia
• Paget disease juvenile type
• Palant cleft palate syndrome
• Panhypopituitarism
• Paraplegia - brachydactyly - cone-shaped epiphysis
• Partial deletion of Y
• Partington-Anderson syndrome
• Pearson's anemia
• Pectus excavatum macrocephaly dysplastic nails
• Pelizaeus-Merzbacher disease, recessive, acute infantile
• Pericardium absent - mental retardation - short stature
• Periodic paralysis, potassium-sensitive, cardiodysrythmic type
• Petit-Fryns syndrome
• Petty-Laxova-Wiedemann syndrome
• Pfeiffer-Palm-Teller syndrome
• PFIC
• Phenylketonuria
• Phocomelia - contractures - absent thumb
• Phocomelia ectrodactyly deafness sinus arrhythmia
• Phocomelia ectrodactyly ear malformation deafness sinus arrhythmia
• PIBIDS syndrome
• Piepkorn karp hickoc syndrome
• Pilotto syndrome
• Pitt-Hopkins syndrome
• Pituitary cancer, childhood
• Pituitary dwarfism 1
• Pituitary tumors, adult
• Plasmalogenes synthesis deficiency isolated
• Plasmalogens synthesis deficiency isolated
• Polydactyly cleft lip palate psychomotor retardation
• Polyneuropathy - mental retardation - acromicria - premature menopause
• Polyneuropathy - Ophthalmoplegia - Leukoencehalopathy - Intestinal Pseudo-Obstruction
• Potocki-Lupski syndrome
• Powell-Chandra-Saal syndrome
• Prader-Willi syndrome
• Premature chromosome condensation with microcephaly and mental retardation
• Primordial short stature - microdontia - opalescent and rootless teeth
• Primrose Syndrome
• Progeria short stature pigmented nevi
• Proud-Levine-Carpenter syndrome
• Proximal tubulopathy - diabetes mellitus - cerebellar ataxia
• Pseudohypoparathyroidism
• Pseudopapilledema - blepharophimosis - hand anomalies
• Pseudoprogeria syndrome
• Pterygia - Mental retardation - Distinctive Craniofacial Features
• Ptosis - coloboma - trigonocephaly
• Pycnodysostosis
• Pyknoachondrogenesis
• Rabson-Mendenhall syndrome
• Radio digito - facial dysplasia
• Radio renal syndrome
• Rajab-Spranger syndrome
• Ramban-Hasharon syndrome
• Rambaud-Galian syndrome
• Ramos-Arroyo Syndrome
• Ramos-ArroyoClark syndrome
• Rathburn disease
• Reardon-Hall-Slaney syndrome
• Recurrent infections - short stature - hypopigmentation - coarse face
• Renal dysplasia - limb defects syndrome
• Renal osteodystrophy
• Renal rickets
• Renoanogenital syndrome
• Renpenning syndrome
• Renpenning syndrome 1
• Rhizomelic chondrodysplasia punctata, type 1
• Rhizomelic chondrodysplasia punctata, type 2
• Rhizomelic chondrodysplasia punctata, type 3
• Rhizomelic dysplasia Patterson Lowry type
• Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
• Rhizomelic syndrome
• Richieri Costa Guion-Almeida syndrome
• Richieri-Costa Da Silva syndrome
• Richieri-Costa Pereira syndrome
• Richieri-Costa-Silveira-Pereira syndrome
• Riddle syndrome
• Rieger anomaly - partial lipodystrophy
• Robinow syndrome, autosomal recessive
• Robinow syndrome, recessive form
• Robinow-like syndrome
• Robinow-Unger syndrome
• Rodrigues blindness
• Roifman syndrome
• Rommen-Mueller-Sybert syndrome
• Rubinstein-Taybi like syndrome
• Sabinas brittle hair syndrome
• Saccharopinuria
• Sackey-Sakati-Aur syndrome
• Sacral agenesis
• Saito-Kuba-Tsuruta syndrome
• Salcedo syndrome
• Sanfilippo syndrome type A
• Sanfilippo syndrome type B
• Satoyoshi syndrome
• Say syndrome
• Say-Barber-Miller syndrome
• Say-Field-Coldwell syndrome
• Say-Meyer syndrome
• Schaap-Taylor-Baraitser syndrome
• Schinzel Syndrome
• Schneckenbecken dysplasia
• Schofer beetz bohl syndrome
• Scoliosis as part of NF
• Seckel syndrome 1
• Seckel syndrome 2
• Seckel syndrome 3
• Seckel-like syndrome, Majoor-Krakauer type
• Seckle syndrome
• Sengers-Hamel-Otten syndrome
• Septo-Optic Dysplasia
• Septooptic dysplasia - digital anomalies
• Serpentine fibula - polycystic kidney syndrome
• Short limb dwarf lethal, Mcalister Crane type
• Short limbs - abnormal face - congenital heart disease
• Short limbs subluxed knees cleft palate
• Short rib-polydactyly syndrome, Majewski type
• Short rib-polydactyly syndrome, Saldino-Noonan type
• Short ribs - craniosynostosis - polysyndactyly
• Short stature - abnormal skin pigmentation - mental retardation
• Short stature - contractures - hypotonia
• Short stature - cranial hyperostosis - hepatomegaly
• Short stature - craniofacial anomalies - genital hypoplasia
• Short stature - dysmorphic face - pelvic scapula dysplasia
• Short stature - hyperkaliemia - acidosis
• Short stature - microcephaly - seizures - deafness
• Short stature - monodactylous - ectrodactyly - cleft palate
• Short stature - pituitary and cerebellar defects - small sella turcica
• Short stature - Robin sequence - cleft mandible - hand anomalies - clubfoot
• Short stature - talipes - natal teeth
• Short stature - valvular heart disease
• Short stature and delayed dental eruption
• Short stature and short, thin, dilacerated dental roots
• Short stature cranial hyperostosis hepatomegaly diabetes
• Short stature deafness neutrophil dysfunction
• Short stature deafness neutrophil dysfunction dysmorphism
• Short stature locking fingers
• Short stature mental retardation eye anomalies
• Short stature mental retardation eye defects
• Short stature valvular heart disease characteristic facies
• Short stature webbed neck heart disease
• Short stature, Brussels type
• Short stature, cranial hyperostosis, hepatomegaly and diabetes
• SHORT Syndrome
• Shoulder girdle defect - mental retardation, familial
• Shprintzen syndorme
• Shprintzen-Goldberg syndrome
• Shwachman syndrome
• SIBIDS syndrome
• Singh-Chhaparwal-Dhanda syndrome
• Single upper central incisor
• Singleton-Merten Syndrome
• Skeletal dysplasia - orofacial anomalies
• Skeletal dysplasia, San Diego type
• Sketetal dysplasia coarse facies mental retardation
• Slavotinek hurst syndrome
• Slavotinek-Pike-Mills-Hurst syndrome
• Smith-Fineman-Myers syndrome 1
• Smith-Fineman-Myers syndrome 2
• Smith-Martin-Dodd syndrome
• Sohval-Soffer syndrome
• Solitary maxillary central incisor, short stature, and choanal atresia
• Sonoda syndrome
• Sparse hair - short stature - skin anomalies
• Spastic paraparesis deafness
• Spastic paraplegia 9, autosomal dominant
• Spastic paraplegia nephritis deafness
• Spinal dysostosis, type Anhalt
• Spinocerebellar ataxia - amyotrophy - deafness
• Spinocerebellar ataxia - dysmorphism
• Spinocerebellar ataxia 13
• Spinocerebellar ataxia, autosomal recessive 5
• Spinocerebellar ataxia, autosomal recessive 6
• Spinocerebellar ataxia-dysmorphism syndrome
• Spondylo-humero-femoral dysplasia
• Spondylocarpotarsal synostosis
• Spondylocostal dysostosis, autosomal recessive
• Spondylocostal dysostosis, autosomal recessive 2
• Spondylocostal dysostosis, autosomal recessive 3
• Spondylocostal dysplasia dominant
• Spondyloenchondrodysplasia
• Spondyloepimetaphyseal dysplasia congenita, Iraqi
• Spondyloepimetaphyseal dysplasia with hypotrichosis
• Spondyloepimetaphyseal dysplasia with multiple dislocations
• Spondyloepimetaphyseal dysplasia, Missouri type
• Spondyloepimetaphyseal dysplasia, X linked with mental deterioration
• Spondyloepimetaphyseal dysplasia, X-linked
• Spondyloepiphyseal dysplasia
• Spondyloepiphyseal dysplasia - brachydactyly and distinctive speech
• Spondyloepiphyseal dysplasia - nephrotic syndrome
• Spondyloepiphyseal dysplasia tarda
• Spondyloepiphyseal dysplasia tarda, autosomal dominant
• Spondyloepiphyseal dysplasia tarda, Toledo type
• Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
• Spondylometaphyseal dysplasia with combined immunodeficiency
• Spondylometaphyseal dysplasia, 'corner fracture' type
• Spondylometaphyseal dysplasia, east-African type
• Spondylometaphyseal dysplasia, X-linked
• Spondyloperipheral dysplasia - short ulna
• Stocco dos Santos syndrome
• Stoll Levy Francort Syndrome
• Stoll-Alembik-Finck syndrome
• Stoll-Geraudel-Chauvin syndrome
• Stratton-Parker syndrome
• Stuve-Wiedemann dysplasia
• Stuve-Wiedemann syndrome
• Subaortic stenosis - short stature syndrome
• Syndactyly type 1 - microcephaly - mental retardation
• Synostosis of talus and calcaneus - short stature
• TAU syndrome
• Taurodontism and disproportionate short stature
• Tel-Hashomer camptodactyly syndrome
• Theodor-Hertz-Goodman syndrome
• Thompson-Baraitser syndrome
• Thong-Douglas-Ferrante syndrome
• Thoracic dysplasia - hydrocephalus syndrome
• Thoracolimb dysplasia, Rivera type
• Thrombocytopathy - asplenia - miosis
• Thrombocytopenia - cerebellar hypoplasia - short stature
• Thrombocytopenia - Robin sequence
• Thumb absent - short stature - immune deficiency
• Thumb deformity, alopecia, pigmentation anomaly
• Thyroid agenesis
• Thyrotropin deficiency, isolated
• Toriello-Higgins-Miller syndrome
• Trichoscyphodysplasia
• Trichothiodystrophy - sun sensitivity
• Trigonocephaly - bifid nose - acral anomalies
• Trigonocephaly - ptosis - mental retardation
• Trisomy 12 mosaicism
• Trisomy 21 mosaicism
• Trisomy 3 mosaicism
• Tsukuhara syndrome
• Tucker syndrome
• Turner Syndrome
• Uniparental disomy
• Uniparental disomy 13
• Uniparental disomy of 11
• Uniparental disomy of 13
• Uniparental disomy of 2
• Uniparental disomy of 6
• Uniparental disomy, paternal, chromosome 14
• Unusual facies, mental retardation, short stature, hemolytic anemia and delayed puberty
• Unusual facies, Myelodysplasia and immunodeficiency
• Unusual facies, short stature, enamel hypoplasia, stiff joints and high-pitched voice
• Unusual facies, short webbed neck, mental retardation, short stature
• Upton Young syndrome
• Urban rogers meyer syndrome
• Urocanase deficiency
• Van Der Bosh syndrome
• Van Goethem syndrome
• Vasquez Hurst Sotos syndrome
• Velocardiofacial syndrome
• Velofacioskeletal syndrome
• Verloes-David Syndrome
• Verloes-Deprez syndrome
• Viljone Kallis Voges syndrome
• Watson syndrome
• Weaver Johnson syndrome
• Weismann-Netter-Stuhl Syndrome
• Wellesley Carmen French syndrome
• Wellesley-Carman-French Syndrome
• Wells Jankovic syndrome
• Werner syndrome
• White matter hypoplasia corpus callosum agenesia mental retardation
• Wiedemann Grosse Dibbern syndrome
• Winchester Syndrome
• Winkelmann Syndrome
• WT limb blood syndrome
• X chromosome, duplication Xq13 1 q21 1
• X chromosome, monosomy Xp22 pter
• X chromosome, monosomy Xq28
• X chromosome, trisomy 26-28
• X chromosome, trisomy Xp3
• X chromosome, trisomy Xpter Xq13
• X chromosome, trisomy Xq
• X chromosome, trisomy Xq25
• X-Linked Agammaglobulinemia
• X-linked mental retardation craniofacial abnormal microcepahly club
• Xeroderma pigmentosum, type 1
• Xeroderma pigmentosum, type 2
• Xylosylprotein 4-beta-galactosyltransferase (XGPT) deficiency
• Young Hughes syndrome
• Zellweger-like syndrome, without peroxisomal anomalies
• Zerres Rietschel Majewski syndrome

Medical news summaries relating to Short stature - hyperkaliemia - acidosis:

The following medical news items are relevant to causes of Short stature - hyperkaliemia - acidosis:

• Wolf-Hirschhorn Syndrome, rare genetic disease
• More news »

Related information on causes of Short stature - hyperkaliemia - acidosis:

As with all medical conditions, there may be many causal factors. Further relevant information on causes of Short stature - hyperkaliemia - acidosis may be found in:

• Hidden causes of Short stature - hyperkaliemia - acidosis

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