Experimental Factor Ontology
6843 terms(s) returned
| Term Type: | Record: 6501 to 6550 of 6843 Records | Page: 131 of 137, First Previous Next Last | Show Records Per Page |
- autonomic nervous system disorder
- autonomic nervous system neoplasm
- autonomic neuropathy
- autophagy protein 5
- autophagy protein 5 (human)
- autophagy-related protein 16-1
- autopod
- autosomal agammaglobulinemia
- autosomal anomaly
- autosomal dominant Alport syndrome
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
- autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
- autosomal dominant Charcot-Marie-Tooth disease type 2K
- autosomal dominant Charcot-Marie-Tooth disease type 2M
- autosomal dominant Charcot-Marie-Tooth disease type 2W
- autosomal dominant Ehlers-Danlos syndrome, vascular type
- autosomal dominant Emery-Dreifuss muscular dystrophy
- autosomal dominant Kenny-Caffey syndrome
- autosomal dominant Robinow syndrome
- autosomal dominant aplasia and myelodysplasia
- autosomal dominant brachyolmia
- autosomal dominant cataract
- autosomal dominant centronuclear myopathy
- autosomal dominant cerebellar ataxia
- autosomal dominant cerebellar ataxia type I
- autosomal dominant cerebellar ataxia type III
- autosomal dominant cerebellar ataxia type IV
- autosomal dominant cerebellar ataxia, deafness and narcolepsy
- autosomal dominant childhood-onset proximal spinal muscular atrophy
- autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
- autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
- autosomal dominant chondrodysplasia punctata
- autosomal dominant coarctation of aorta
- autosomal dominant common variable immunodeficiency
- autosomal dominant compelling helio-ophthalmic outburst syndrome
- autosomal dominant complex spastic paraplegia
- autosomal dominant cutis laxa
- autosomal dominant deafness - onychodystrophy syndrome
- autosomal dominant dilated cardiomyopathy
- autosomal dominant disease
- autosomal dominant distal myopathy
- autosomal dominant distal renal tubular acidosis
- autosomal dominant dopa-responsive dystonia
- autosomal dominant epidermolytic ichthyosis
- autosomal dominant epilepsy with auditory features
- autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome
- autosomal dominant hereditary axonal motor and sensory neuropathy
- autosomal dominant hereditary sensory and autonomic neuropathy
- autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- autosomal dominant hyperinsulinism due to SUR1 deficiency
