Experimental Factor Ontology
1206 terms(s) returned
Term Type: | Record: 1051 to 1100 of 1206 Records | Page: 22 of 25, First Previous Next Last | Show Records Per Page |
- 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 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 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 type 9B
- 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 cutis laxa type 1
- autosomal recessive cutis laxa type 2
- autosomal recessive cutis laxa type 2, classic type
- autosomal recessive cutis laxa type 2A
- autosomal recessive cutis laxa type 2B
- autosomal recessive degenerative and progressive cerebellar ataxia
- autosomal recessive distal osteolysis syndrome
- autosomal recessive distal renal tubular acidosis
- autosomal recessive distal spinal muscular atrophy 1
- autosomal recessive distal spinal muscular atrophy 2
- autosomal recessive dyskeratosis congenita 4
- autosomal recessive epidermolytic ichthyosis
- autosomal recessive faciodigitogenital syndrome
- autosomal recessive familial Mediterranean fever
- autosomal recessive frontotemporal pachygyria