Experimental Factor Ontology
3875 terms(s) returned
| Term Type: | Record: 3651 to 3700 of 3875 Records | Page: 74 of 78, First Previous Next Last | Show Records Per Page |
- autosomal dominant optic atrophy, classic form
- autosomal dominant osteopetrosis
- autosomal dominant osteopetrosis 1
- autosomal dominant osteopetrosis 2
- autosomal dominant osteosclerosis, Worth type
- autosomal dominant palmoplantar keratoderma and congenital alopecia
- autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- autosomal dominant polycystic liver disease
- autosomal dominant popliteal pterygium syndrome
- autosomal dominant primary microcephaly
- autosomal dominant prognathism
- autosomal dominant progressive external ophthalmoplegia
- autosomal dominant progressive nephropathy with hypertension
- autosomal dominant proximal renal tubular acidosis
- autosomal dominant proximal spinal muscular atrophy
- autosomal dominant pseudohypoaldosteronism type 1
- autosomal dominant pure spastic paraplegia
- autosomal dominant retinitis pigmentosa
- 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
