Experimental Factor Ontology
135 terms(s) returned
| Term Type: | Record: 1 to 50 of 135 Records | Page: 1 of 3, First Previous Next Last | Show Records Per Page |
- GM2-gangliosidosis, AB variant
- Gamma-aminobutyric acid transaminase deficiency
- Gaucher disease - ophthalmoplegia - cardiovascular calcification
- Gaucher disease type 1
- Gaucher disease type 2
- Gaucher disease type 3
- Generalized arterial calcification of infancy
- Generalized congenital lipodystrophy with myopathy
- Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
- Generalized epilepsy - paroxysmal dyskinesia
- Generalized epilepsy with febrile seizures-plus
- Generalized junctional epidermolysis bullosa, non-Herlitz type
- Generalized pseudohypoaldosteronism type 1
- Genetic 46,XX disorder of sex development
- Genetic 46,XY disorder of sex development
- Genetic 46,XY disorder of sex development of endocrine origin
- Genetic acrokeratoderma
- Genetic bone tumor
- Genetic branchial arch or oral-acral syndrome
- Genetic cardiac tumor
- Genetic central nervous system malformation
- Genetic cerebellar malformation
- Genetic cerebral malformation
- Genetic cerebrovascular dementia
- Genetic chronic primary adrenal insufficiency
- Genetic congenital limb malformation
- Genetic cranial malformation
- Genetic dermis elastic tissue disorder
- Genetic developmental defect of the eye
- Genetic digestive tract malformation
- Genetic digestive tract tumor
- Genetic disorder of sex development
- Genetic disorder of sex development of gynecological interest
- Genetic endocrine tumor
- Genetic epidermal disorder
- Genetic erythrokeratoderma
- Genetic eye tumor
- Genetic frontotemporal degeneration with dementia
- Genetic glomerular disease
- Genetic gynecological tumor
- Genetic hyperferritinemia without iron overload
- Genetic hyperpigmentation of the skin
- Genetic hypopigmentation of the skin
- Genetic immune deficiency with skin involvement
- Genetic interstitial lung disease
- Genetic intestinal disease
- Genetic intestinal disease due to fat malabsorption
- Genetic intractable diarrhea of infancy
- Genetic keratinization disorder associated with ocular features
- Genetic lens and zonula anomaly
