Common causes of Facial feature symptoms
Introduction:
This information shows the various causes of Facial feature symptoms, and how common these diseases
or conditions are in the general population.
This is not a direct indication as to how commonly these diseases are the actual cause
of Facial feature symptoms, but gives a relative idea as to how frequent these diseases are seen overall.
1
diseases that are "uncommon".
8
diseases that are "rare".
6
diseases that are "rare".
231
diseases without any prevalence information.
Causes of Facial feature symptoms that are uncommon
The following causes of Facial feature symptoms are diseases or conditions that
affect more than 200,000 people, but less than 1 million people in the USA:
Causes of Facial feature symptoms that are rare
The offical US government definition of a "rare" disease is one that
affects 200,000 people or less.
The following causes of Facial feature symptoms appear in the population
at a rate of less than 200,000 people per year in the USA:
Causes of Facial feature symptoms that are very rare
The following causes of Facial feature symptoms appear in the population
at a rate of substantially less than 200,000 people per year in the USA:
Causes of Facial feature symptoms without any prevalence information
The following causes of Facial feature symptoms are ones for which
we do not have any prevalence information.
- 11q Partial Trisomy - facial abnormalities
- 14q+ syndrome - large face
- Acrocephalopolydactyly - facial abnormalities
- Acromegaly due to growth hormone-secreting pituitary adenoma - Coarse facial features
- Adducted thumb syndrome recessive form - craniofacial abnormalities
- Adducted thumbs - arthrogryposis, Christian type - craniofacial abnormalities
- Adrenal adenoma, familial - large face
- Adrenal Cancer - large face
- Adrenal Cortex Neoplasms - large face
- Adrenal gland hyperfunction - large face
- Adrenal incidentaloma - large face
- Adrenocortical carcinoma - large face
- Alagille Syndrome - unusual facial features
- Alpha-mannosidosis type II - coarse facial features
- Amniotic Bands - flattened face
- Aortic supravalvular stenosis - facial abnormalities
- Arthrogryposis multiplex congenita type 2B - narrow face
- Arthrogryposis, distal, type 2B - narrow face
- Aspartylglucosaminidase deficiency - coarse facial features
- Aspartylglucosaminuria - coarse facial features
- Aspartylglycosaminuria - coarse facial features
- Ataxia - diabetes - goiter - gonadal insufficiency - narrow face
- Bangstad syndrome - narrow face
- Battaglia Neri syndrome - coarse facial features
- Beemer-Ertbruggen syndrome - characteristic facial features
- Bird-headed dwarfism with progressive ataxia, Insulin-resistant diabetes, goiter and primary gonadal insufficiency - narrow face
- BOD syndrome - unusual facial features
- Boomerang dysplasia - characteristic facial features
- Borjeson Syndrome - coarse facial features
- Boscherini-Galasso-Manca-Bitti syndrome - facial abnormalities
- Bosviel syndrome - characteristic facial features
- Camptodactyly syndrome, Guadalajara type III - characteristic facial features
- CATCH 22 - facial abnormalities
- Caudal appendage - deafness - unusual facial features
- Cerebellar vermis hypoplasia - oligophrenia - congenital ataxia - coloboma - hepatic fibrosis - unusual facial features
- Cerebro-oculo-nasal syndrome - large face
- Cervenka's syndrome - flattened midface
- Chondrodysplasia punctata, non rhizomelic type - facial abnormalities
- Chromosome 1, pter-p36 - coarse facial features
- Chromosome 1, uniparental disomy 1q12 q21 - Narrow face
- Chromosome 10, trisomy 10p - Narrow face
- Chromosome 10p duplication syndrome - narrow face
- Chromosome 11, deletion 11p - Narrow face
- Chromosome 11, Partial Trisomy 11q - facial abnormalities
- Chromosome 12p partial deletion - craniofacial abnormalities
- Chromosome 14q deletion syndrome - narrow face
- Chromosome 14q, partial deletion - narrow face
- Chromosome 18, trisomy 18q - narrow face
- Chromosome 1p deletion syndrome - narrow face
- Chromosome 20, trisomy - unusual facial features
- Chromosome 21 Ring - facial abnormalities
- Chromosome 2p deletion syndrome - narrow face
- Chromosome 4, Monosomy Distal 4q - facial abnormalities
- Chromosome 6, monosomy 6q - Coarse facial features
- Chromosome 6q deletion syndrome - coarse facial features
- Chromosome 7, monosomy 7q3 - large face
- Chromosome 9, partial trisomy 9p - flattened midface
- Chromosome 9, Trisomy 9p (Multiple Variants) - facial abnormalities
- Chromosome 9/mosaic - narrow face
- Cleft lip and palate - malrotation - cardiopathy - characteristic facial features
- COACH syndrome - unusual facial features
- Coarse face - hypotonia - constipation - coarse facial features
- Complex 5 mitochondrial respiratory chain deficiency - unusual facial features
- Congenital disorder of glycosylation type 1/IIX - unusual facial features
- Congenital disorder of glycosylation type 1H - unusual facial features
- Congenital hypothyroidism - distorted facial features
- Corneal anesthesia deafness intellectual deficit - unusual facial features
- Corneal anesthesia deafness mental retardation - unusual facial features
- Corneal hypesthesia deafness intellectual deficit - unusual facial features
- Cornelia de Lange Syndrome - facial abnormalities
- Corpus callosum dysgenesis X-linked recessive - unusual facial features
- Cranioacrofacial syndrome - narrow face
- Crisponi syndrome - large face
- Cushing's syndrome - rounded face
- Cutis Laxa with Bone Dystrophy - flattened face
- Cutis Laxa with Growth and Developmental Delay - flattened face
- Cutis Laxa with or without Congenital Disorder of Glycosylation - flattened face
- Cutis Laxa, Autosomal Recessive, Type IIA - flattened face
- Cutis Laxa, Debre Type - flattened face
- Cutis laxa, recessive type 2 - flattened face
- Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures - narrow face
- Deletion 11p - Narrow face
- Deletion 11q - unusual facial features
- Deletion 6q - Coarse facial features
- Diflucan - Teratogenic Agent - craniofacial abnormalities
- DiGeorge syndrome - characteristic facial features
- DiGeorge's syndrome - characteristic facial features
- Distal Trisomy 11q - facial abnormalities
- Dup (5)(q31-qter) - facial abnormalities
- Dup (5)(q32-qter) - facial abnormalities
- Dup (5)(q33-qter) - facial abnormalities
- Duplication 10p - Narrow face
- Duplication 9p partial - flattened midface
- Dyggve-Melchior-Clausen Syndrome - coarse facial features
- Dysmorphism - cleft palate - loose skin - narrow face
- Eccentrochondrodysplasia - unusual facial features
- Ectodermal dysplasia - alopecia - preaxial polydactyly - facial abnormalities
- Ectopic acromegaly - Coarse facial features
- Edinburgh malformation syndrome - facial abnormalities
- Ehlers-Danlos syndrome, Beasley Cohen type - narrow face
- Fetal alcohol syndrome - characteristic facial features
- Fluconazole - Teratogenic Agent - craniofacial abnormalities
- Fucosidosis type 1 - coarse facial features
- Fucosidosis type II - coarse facial features
- Fumaric aciduria - unusual facial features
- Functioning pancreatic endocrine tumor - large face
- Gangliosidosis generalized GM1, type 1 - coarse facial features
- Gangliosidosis GM1 type 3 - coarse facial features
- Gangliosidosis, generalized GM1 type 3 - coarse facial features
- GM1 gangliosidosis - coarse facial features
- Goldberg syndrome - coarse facial features
- Hydantoin - Teratogenic Agent - unusual facial features
- Hyde-Forster-Mccarthy-Berry syndrome - coarse facial features
- Hyper IgE - coarse facial features
- Hyperadrenalism - large face
- Hyperglycerolemia, infantile form - characteristic facial features
- Hypertelorism with esophageal abnormality and hypospadias - craniofacial abnormalities
- Hyperthermia induced defects - craniofacial abnormalities
- Hypomelanosis of Ito - coarse facial features
- Hypospadias - hypertelorism - craniofacial abnormalities
- I cell disease - coarse facial features
- Immunodeficiency due to defect in MAPBP-interacting protein - coarse facial features
- Infantile Refsum Disease - mild facial abnormalities
- Infantile sialic acid storage disorder - coarse facial features
- Job syndrome - coarse facial features
- Kaler-Garrity-Stern syndrome - mild facial abnormalities
- Kaufman oculocerebrofacial syndrome - narrow face
- Langer-Nishino-Yamaguchi syndrome - facial abnormalities
- Mannosidosis, alpha B lysosomal - coarse facial features
- Marfan Syndrome type 2 - narrow face
- MASS syndrome - narrow face
- McCune-Albright Syndrome - coarse facial features
- Megarbane syndrome - facial abnormalities
- Megarbane-Jalkh Syndrome - unusual facial features
- Mental retardation - arachnodactyly - hypotonia - telangiectasia - narrow face
- Mental retardation, Smith-Fineman-Myers type - narrow face
- Mental retardation, X-linked - corpus callosum agenesis - spastic quadriparesis - craniofacial abnormalities
- Mental retardation, X-linked - epilepsy - progressive joint contractures - typical face - coarse facial features
- Mental retardation, X-linked, Brooks type - unusual facial features
- Mental retardation, X-linked, Raynaud type - coarse facial features
- Metaphyseal chondrodysplasia, recessive type - large face
- Microcephaly - large face
- Miescher's syndrome - coarse facial features
- Morquio syndrome - coarse facial features
- Morquio syndrome type A - coarse facial features
- Morquio syndrome, type B - coarse facial features
- MPS 3 C - coarse facial features
- MPS 3 D - coarse facial features
- Mucolipidosis III - coarse facial features
- Mucopolysaccharidosis type 2 Hunter syndrome- mild form - coarse facial features
- Mucopolysaccharidosis type 2 Hunter syndrome- severe form - coarse facial features
- Mucopolysaccharidosis type 3 - coarse facial features
- Mucopolysaccharidosis type 6 - coarse facial features
- Mucopolysaccharidosis type 7 Sly syndrome - coarse facial features
- Mucopolysaccharidosis type I Hurler syndrome - coarse facial features
- Mucopolysaccharidosis type I Hurler/Scheie syndrome - coarse facial features
- Mucopolysaccharidosis type I Scheie syndrome - coarse facial features
- Mucopolysaccharidosis Type III - coarse facial features
- Multicentric osteolysis - nodulosis - arthropathy - coarse facial features
- Multiple endocrine abnormalities - adenylyl cyclase dysfunction - coarse facial features
- Multiple endocrine neoplasia type 2b - coarse facial features
- Multiple pterygium syndrome - facial abnormalities
- Multiple pterygium syndrome, autosomal recessive - facial abnormalities
- Multiple synostosis syndrome - narrow face
- Muscular dystrophy - white matter spongiosis - narrow face
- N-acetyl-alpha-glucosaminidase sulfamidase deficiency - coarse facial features
- Nasopharyngeal teratoma with Dandy-Walker - diaphragmatic hernia - large face
- Neonatal ALD - facial abnormalities
- Nephroblastomatosis - fetal ascites - macrosomia - wilms tumor - unusual facial features
- Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor - unusual facial features
- Neuraminidase deficiency, type II, juvenile form - coarse facial features
- Neuritis with brachial predilection - narrow face
- Nodulosis-arthropathy-osteolysis syndrome - coarse facial features
- Nonkeratan-sulfate-excreting Morquio syndrome - coarse facial features
- Oculorenocerebellar syndrome - narrow face
- Opitz syndrome , X-linked - craniofacial abnormalities
- Opsismodysplasia - facial abnormalities
- Orofaciodigital syndrome, Gabrielli type - facial abnormalities
- Osteopetrosis lethal - craniofacial abnormalities
- Osteosclerosis, abnormalities of nervous system and meninges - narrow face
- Paris-Trousseau thrombocytopenia - facial abnormalities
- Pituitary cancer, childhood - large face
- Pituitary tumors, adult - large face
- Pollitt syndrome - unusual facial features
- Prolidase deficiency - characteristic facial features
- Pycnodysostosis - craniofacial abnormalities
- Ramos-Arroyo Syndrome - unusual facial features
- Ramos-ArroyoClark syndrome - unusual facial features
- Renpenning syndrome - narrow face
- Renpenning syndrome 1 - narrow face
- Rhizomelic dysplasia Patterson Lowry type - large face
- Richieri Costa Guion Almeida Cohen syndrome - narrow face
- Robin sequence and oligodactyly - narrow face
- Robin sequence oligodactyly - narrow face
- Say-Barber-Miller syndrome - unusual facial features
- SCARF syndrome - facial abnormalities
- Seckel syndrome 1 - narrow face
- Seckle syndrome - narrow face
- Short stature - valvular heart disease - large face
- Sialidosis type II, congenital - coarse facial features
- Sialidosis type II, infantile - coarse facial features
- Sialuria syndrome - coarse facial features
- Simpson-Golabi-Behmel syndrome - coarse facial features
- Simpson-Golabi-Behmel syndrome, type 1 (SGBS1) - coarse facial features
- Skeletal dysplasia - coarse facies - mental retardation - coarse facial features
- Skeletal dysplasia - mental retardation - craniofacial abnormalities
- Sketetal dysplasia coarse facies mental retardation - coarse facial features
- Smith-Fineman-Myers syndrome 1 - narrow face
- Spondyloepimetaphyseal Dysplasia, Aggrecan Type - craniofacial abnormalities
- Spondyloepimetaphyseal dysplasia, genevieve type - coarse facial features
- Sulfatidosis juvenile, Austin type - coarse facial features
- Trichorhinophalangeal syndrome type 3 - unusual facial features
- Trichorrhexis nodosa syndrome - unusual facial features
- Trichothiodystrophy, type C - unusual facial features
- Trichothiodystrophy-neurocutaneous Syndrome - unusual facial features
- Trichothiodystrophy-neurotrichocutaneous Syndrome of Pollitt - unusual facial features
- Trisomy 18 mosaicism - unusual facial features
- Van Bogaert-Hozay syndrome - Facial abnormalities
- Van Maldergem Wetzburger Verloes syndrome - Facial abnormalities
- Van Regemorter Pierquin Vamos syndrome - Facial abnormalities
- Verloes Gillerot Fryns syndrome - Facial abnormalities
- Wagner-Stickler Syndrome - flattened face
- WAGR Syndrome - narrow face
- Weatherall syndrome - facial abnormalities
- Wilkie Taylor Scambler syndrome - narrow face
- Wilms tumor - aniridia - genitourinary anomalies - mental retardation - narrow face
- Winchester Syndrome - coarse facial features
- Winter Harding Hyde syndrome - Facial abnormalities
- Yim Ebbin syndrome - Facial abnormalities
- Zazam Sheriff Phillips syndrome - Facial abnormalities
- Zerres Rietschel Majewski syndrome - Facial abnormalities
All Causes of Facial feature symptoms
The full list of all possible causes for Facial feature symptoms described in various sources is as follows:
See full list of possible disease causes of Facial feature symptoms
» Next page: Glossary
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