Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 3851 to 3900 of 11113 Records | Page: 78 of 223, First Previous Next Last | Show Records Per Page |
- obsolete_autosomal anomaly
- obsolete_autosomal dominant Alport syndrome
- obsolete_autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
- obsolete_autosomal dominant Charcot-Marie-Tooth disease type 2K
- obsolete_autosomal dominant Charcot-Marie-Tooth disease type 2M
- obsolete_autosomal dominant Emery-Dreifuss muscular dystrophy
- obsolete_autosomal dominant Kenny-Caffey syndrome
- obsolete_autosomal dominant Opitz G/BBB syndrome
- obsolete_autosomal dominant Robinow syndrome
- obsolete_autosomal dominant aplasia and myelodysplasia
- obsolete_autosomal dominant brachyolmia
- obsolete_autosomal dominant centronuclear myopathy
- obsolete_autosomal dominant cerebellar ataxia
- obsolete_autosomal dominant cerebellar ataxia, deafness and narcolepsy
- obsolete_autosomal dominant childhood-onset proximal spinal muscular atrophy
- obsolete_autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
- obsolete_autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
- obsolete_autosomal dominant chondrodysplasia punctata
- obsolete_autosomal dominant complex spastic paraplegia
- obsolete_autosomal dominant congenital benign spinal muscular atrophy
- obsolete_autosomal dominant cutis laxa
- obsolete_autosomal dominant diffuse mutilating palmoplantar keratoderma
- obsolete_autosomal dominant distal hereditary motor neuropathy
- obsolete_autosomal dominant distal myopathy
- obsolete_autosomal dominant distal renal tubular acidosis
- obsolete_autosomal dominant hereditary axonal motor and sensory neuropathy
- obsolete_autosomal dominant hereditary demyelinating motor and sensory neuropathy
- obsolete_autosomal dominant hereditary sensory and autonomic neuropathy
- obsolete_autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- obsolete_autosomal dominant hyperinsulinism due to SUR1 deficiency
- obsolete_autosomal dominant hypocalcemia
- obsolete_autosomal dominant hypohidrotic ectodermal dysplasia
- obsolete_autosomal dominant hypophosphatemic rickets
- obsolete_autosomal dominant intermediate Charcot-Marie-Tooth disease
- obsolete_autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
- obsolete_autosomal dominant isolated diffuse palmoplantar keratoderma
- obsolete_autosomal dominant keratitis
- obsolete_autosomal dominant limb-girdle muscular dystrophy type 1F
- obsolete_autosomal dominant limb-girdle muscular dystrophy type 1G
- obsolete_autosomal dominant limb-girdle muscular dystrophy type 1H
- obsolete_autosomal dominant macrothrombocytopenia
- obsolete_autosomal dominant medullary cystic kidney disease with or without hyperuricemia
- obsolete_autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
- obsolete_autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
- obsolete_autosomal dominant myoglobinuria
- obsolete_autosomal dominant nocturnal frontal lobe epilepsy
- obsolete_autosomal dominant non-syndromic intellectual disability
- obsolete_autosomal dominant omodysplasia
- obsolete_autosomal dominant optic atrophy
- obsolete_autosomal dominant optic atrophy and peripheral neuropathy
