Experimental Factor Ontology
94474 terms(s) returned
| Term Type: | Record: 3801 to 3850 of 94474 Records | Page: 77 of 1890, First Previous Next Last | Show Records Per Page |
- Autosomal dominant Charcot-Marie-Tooth disease type 2N
- Autosomal dominant Charcot-Marie-Tooth disease type 2O
- Autosomal dominant Charcot-Marie-Tooth disease type 2Q
- Autosomal dominant Larsen syndrome
- Autosomal dominant beta2-microglobulinic amyloidosis
- Autosomal dominant cerebellar ataxia type 1
- Autosomal dominant cerebellar ataxia type 2
- Autosomal dominant cerebellar ataxia type 3
- Autosomal dominant cerebellar ataxia type 4
- Autosomal dominant childhood-onset cortical cataract
- Autosomal dominant deafness-onychodystrophy syndrome
- Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature
- Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
- Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
- Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
- Autosomal dominant focal dystonia, DYT25
- Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering
- Autosomal dominant hyper-IgE syndrome
- Autosomal dominant inheritance
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
- Autosomal dominant limb-girdle muscular dystrophy
- Autosomal dominant limb-girdle muscular dystrophy type 1B
- Autosomal dominant limb-girdle muscular dystrophy type 1C
- Autosomal dominant limb-girdle muscular dystrophy type 1D
- Autosomal dominant limb-girdle muscular dystrophy type 1E
- Autosomal dominant medullary cystic kidney disease with hyperuricemia
- Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency
- Autosomal dominant methemoglobinemia
- Autosomal dominant microcephaly
- Autosomal dominant multiple pterygium syndrome
- Autosomal dominant nail dysplasia
- Autosomal dominant optic atrophy and cataract
- Autosomal dominant optic atrophy and late-onset deafness
- Autosomal dominant optic atrophy, classic type
- Autosomal dominant osteopetrosis type 1
- Autosomal dominant primary hypomagnesemia with hypocalciuria
- Autosomal dominant spastic paraplegia type 10
- Autosomal dominant spastic paraplegia type 12
- Autosomal dominant spastic paraplegia type 13
- Autosomal dominant spastic paraplegia type 17
- Autosomal dominant spastic paraplegia type 19
- Autosomal dominant spastic paraplegia type 29
- Autosomal dominant spastic paraplegia type 3
- Autosomal dominant spastic paraplegia type 31
- Autosomal dominant spastic paraplegia type 36
