Experimental Factor Ontology
3807 terms(s) returned
Term Type: Class | Record: 3601 to 3650 of 3807 Records | Page: 73 of 77, First Previous Next Last | Show Records Per Page |
- autosomal dominant rhegmatogenous retinal detachment
- autosomal dominant secondary polycythemia
- autosomal dominant sensory ataxia 1
- autosomal dominant severe congenital neutropenia
- autosomal dominant sideroblastic anemia
- autosomal dominant slowed nerve conduction velocity
- autosomal dominant spastic ataxia
- autosomal dominant spastic paraplegia type 9
- autosomal dominant spondylocostal dysostosis
- autosomal dominant striatal neurodegeneration type 1
- autosomal dominant titinopathy
- autosomal dominant trichoodontoonychodysplasia-syndactyly
- autosomal dominant vibratory urticaria
- autosomal dominant vitreoretinochoroidopathy
- autosomal dominant wooly hair
- autosomal erythropoietic protoporphyria
- autosomal genetic disease
- autosomal recessive Alport syndrome
- autosomal recessive Ehlers-Danlos syndrome, vascular type
- autosomal recessive Emery-Dreifuss muscular dystrophy
- autosomal recessive Kenny-Caffey syndrome
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- autosomal recessive Parkinson disease 14
- autosomal recessive Robinow syndrome
- autosomal recessive amelia
- autosomal recessive ataxia due to PEX10 deficiency
- autosomal recessive ataxia due to ubiquinone deficiency
- autosomal recessive ataxia, Beauce type
- autosomal recessive axonal hereditary motor and sensory neuropathy
- autosomal recessive bestrophinopathy
- autosomal recessive brachyolmia
- autosomal recessive centronuclear myopathy
- autosomal recessive cerebellar ataxia
- autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
- autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
- autosomal recessive cerebellar ataxia with late-onset spasticity
- autosomal recessive cerebellar ataxia-blindness-deafness syndrome
- autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
- autosomal recessive cerebral atrophy
- autosomal recessive complex spastic paraplegia
- autosomal recessive complex spastic paraplegia type 9B
- autosomal recessive cone rod dystrophy
- autosomal recessive congenital cerebellar ataxia
- autosomal recessive congenital ichthyosis
- autosomal recessive congenital ichthyosis 11
- autosomal recessive congenital ichthyosis 4A
- autosomal recessive congenital ichthyosis 4B
- autosomal recessive congenital stationary night blindness