Experimental Factor Ontology
6213 terms(s) returned
| Term Type: | Record: 101 to 150 of 6213 Records | Page: 3 of 125, First Previous Next Last | Show Records Per Page |
- Amaurosis - hypertrichosis
- Amelo-cerebro-hypohidrotic syndrome
- Amelo-onycho-hypohidrotic syndrome
- Amelogenesis imperfecta and gingival hyperplasia syndrome
- Aminoacylase deficiency
- Amish nemaline myopathy
- Amniotic bands
- Anemia due to adenosine triphosphatase deficiency
- Aneurysm - osteoarthritis syndrome
- Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
- Aniridia - absent patella
- Aniridia - cerebellar ataxia - intellectual disability
- Aniridia - ptosis - intellectual disability - familial obesity
- Aniridia - renal agenesis - psychomotor retardation
- Aniridia-intellectual disability syndrome
- Ankyloblepharon - ectodermal defects - cleft lip/palate
- Ankyloblepharon filiforme - imperforate anus
- Ankyloblepharon filiforme adnatum - cleft palate
- Anonychia - microcephaly
- Anonychia - onychodystrophy
- Anonychia congenita totalis
- Anophthalmia - megalocornea - cardiopathy - skeletal anomalies
- Anophthalmia/microphthalmia - esophageal atresia
- Anterior polar cataract
- Aortic arch anomaly - peculiar facies - intellectual disability
- Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis
- Aphalangy - syndactyly - microcephaly
- Aphonia - deafness - retinal dystrophy - bifid halluces - intellectual disability
- Aplasia cutis - myopia
- Aplasia cutis congenita - intestinal lymphangiectasia
- Arachnodactyly - abnormal ossification - intellectual disability
- Arachnodactyly - intellectual disability - dysmorphism
- Arginine:glycine amidinotransferase deficiency
- Argininemia
- Arnold-Chiari malformation type I
- Arnold-Chiari malformation type II
- Arrhinia - choanal atresia - microphthalmia
- Arrhythmogenic right ventricular dysplasia
- Arthrogryposis - hyperkeratosis, lethal form
- Arthrogryposis - renal dysfunction - cholestasis
- Arthrogryposis - severe scoliosis
- Arthrogryposis multiplex congenita - whistling face
- Arthrogryposis with oculomotor limitation and electroretinal anomalies
- Arthrogryposis-like hand anomaly - sensorineural deafness
- Ataxia - hypogonadism - choroidal dystrophy
- Ataxia - oculomotor apraxia type 1
- Ataxia - pancytopenia
- Ataxia - tapetoretinal degeneration
- Ataxia with dementia
- Ataxia with vitamin E deficiency
