Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 3901 to 3950 of 11113 Records | Page: 79 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_autosomal dominant optic atrophy plus syndrome
- obsolete_autosomal dominant osteosclerosis, Worth type
- obsolete_autosomal dominant palmoplantar keratoderma and congenital alopecia
- obsolete_autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- obsolete_autosomal dominant popliteal pterygium syndrome
- obsolete_autosomal dominant prognathism
- obsolete_autosomal dominant progressive external ophthalmoplegia
- obsolete_autosomal dominant progressive nephropathy with hypertension
- obsolete_autosomal dominant proximal renal tubular acidosis
- obsolete_autosomal dominant proximal spinal muscular atrophy
- obsolete_autosomal dominant pure spastic paraplegia
- obsolete_autosomal dominant rhegmatogenous retinal detachment
- obsolete_autosomal dominant secondary polycythemia
- obsolete_autosomal dominant severe congenital neutropenia
- obsolete_autosomal dominant slowed nerve conduction velocity
- obsolete_autosomal dominant spastic ataxia
- obsolete_autosomal dominant spastic paraplegia type 9
- obsolete_autosomal dominant spondylocostal dysostosis
- obsolete_autosomal dominant trichoodontoonychodysplasia-syndactyly
- obsolete_autosomal dominant vitreoretinochoroidopathy
- obsolete_autosomal ichthyosis syndrome
- obsolete_autosomal recessive Alport syndrome
- obsolete_autosomal recessive Emery-Dreifuss muscular dystrophy
- obsolete_autosomal recessive Kenny-Caffey syndrome
- obsolete_autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- obsolete_autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- obsolete_autosomal recessive Robinow syndrome
- obsolete_autosomal recessive Stickler syndrome
- obsolete_autosomal recessive amelia
- obsolete_autosomal recessive ataxia due to PEX10 deficiency
- obsolete_autosomal recessive ataxia due to ubiquinone deficiency
- obsolete_autosomal recessive ataxia, Beauce type
- obsolete_autosomal recessive bestrophinopathy
- obsolete_autosomal recessive centronuclear myopathy
- obsolete_autosomal recessive cerebellar ataxia
- obsolete_autosomal recessive cerebellar ataxia with late-onset spasticity
- obsolete_autosomal recessive cerebral atrophy
- obsolete_autosomal recessive complex spastic paraplegia
- obsolete_autosomal recessive congenital cerebellar ataxia
- obsolete_autosomal recessive congenital ichthyosis
- obsolete_autosomal recessive cutis laxa type 1
- obsolete_autosomal recessive cutis laxa type 2
- obsolete_autosomal recessive cutis laxa type 2, classic type
- obsolete_autosomal recessive cutis laxa type 2A
- obsolete_autosomal recessive cutis laxa type 2B
- obsolete_autosomal recessive degenerative and progressive cerebellar ataxia
- obsolete_autosomal recessive disease
- obsolete_autosomal recessive distal hereditary motor neuropathy
- obsolete_autosomal recessive distal myopathy
- obsolete_autosomal recessive distal osteolysis syndrome
