Experimental Factor Ontology
6782 terms(s) returned
| Term Type: | Record: 6501 to 6550 of 6782 Records | Page: 131 of 136, First Previous Next Last | Show Records Per Page |
- autosomal dominant limb-girdle muscular dystrophy type 1E (DES)
- autosomal dominant limb-girdle muscular dystrophy type 1F
- autosomal dominant limb-girdle muscular dystrophy type 1G
- autosomal dominant limb-girdle muscular dystrophy type 1H
- autosomal dominant macrothrombocytopenia
- autosomal dominant medullary cystic kidney disease with or without hyperuricemia
- autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- autosomal dominant mitochondrial myopathy with exercise intolerance
- autosomal dominant myoglobinuria
- autosomal dominant nebulin-related myopathy
- autosomal dominant nocturnal frontal lobe epilepsy
- autosomal dominant nocturnal frontal lobe epilepsy 5
- autosomal dominant non-syndromic intellectual disability
- autosomal dominant nonsyndromic hearing loss
- autosomal dominant nonsyndromic hearing loss 1
- autosomal dominant nonsyndromic hearing loss 10
- autosomal dominant nonsyndromic hearing loss 11
- autosomal dominant nonsyndromic hearing loss 13
- autosomal dominant nonsyndromic hearing loss 17
- autosomal dominant nonsyndromic hearing loss 28
- autosomal dominant nonsyndromic hearing loss 2A
- autosomal dominant nonsyndromic hearing loss 30
- autosomal dominant nonsyndromic hearing loss 36
- autosomal dominant nonsyndromic hearing loss 3A
- autosomal dominant nonsyndromic hearing loss 3B
- autosomal dominant nonsyndromic hearing loss 40
- autosomal dominant nonsyndromic hearing loss 4A
- autosomal dominant nonsyndromic hearing loss 58
- autosomal dominant nonsyndromic hearing loss 65
- autosomal dominant nonsyndromic hearing loss 69
- autosomal dominant nonsyndromic hearing loss 7
- autosomal dominant nonsyndromic hearing loss 70
- autosomal dominant oculocutaneous albinism
- autosomal dominant omodysplasia
- autosomal dominant optic atrophy
- autosomal dominant optic atrophy and peripheral neuropathy
- autosomal dominant optic atrophy plus syndrome
- 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
- 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
