Experimental Factor Ontology
6843 terms(s) returned
| Term Type: | Record: 2251 to 2300 of 6843 Records | Page: 46 of 137, First Previous Next Last | Show Records Per Page |
- Autoimmune lymphoproliferative syndrome with recurrent viral infections
- Autoimmune polyendocrinopathy type 1
- Autoimmunity
- Autoinflammatory syndrome with immune deficiency
- Autosomal codominant severe lipodystrophic laminopathy
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1
- Autosomal dominant Charcot-Marie-Tooth disease type 2A2
- Autosomal dominant Charcot-Marie-Tooth disease type 2B
- Autosomal dominant Charcot-Marie-Tooth disease type 2C
- Autosomal dominant Charcot-Marie-Tooth disease type 2D
- Autosomal dominant Charcot-Marie-Tooth disease type 2E
- Autosomal dominant Charcot-Marie-Tooth disease type 2F
- Autosomal dominant Charcot-Marie-Tooth disease type 2I
- Autosomal dominant Charcot-Marie-Tooth disease type 2J
- Autosomal dominant Charcot-Marie-Tooth disease type 2L
- 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
