Experimental Factor Ontology
3199 terms(s) returned
| Term Type: | Record: 2901 to 2950 of 3199 Records | Page: 59 of 64, First Previous Next Last | Show Records Per Page |
- muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome
- muscular dystrophy, congenital, with cataracts and intellectual disability
- muscular dystrophy, congenital, with or without seizures
- muscular dystrophy, congenital, with rapid progression
- muscular dystrophy, limb-girdle, autosomal dominant
- muscular dystrophy, limb-girdle, autosomal dominant 4
- muscular dystrophy, limb-girdle, autosomal recessive 23
- muscular dystrophy, limb-girdle, autosomal recessive 27
- muscular dystrophy, limb-girdle, autosomal recessive 28
- muscular dystrophy-dystroglycanopathy
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
- muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
- muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
- muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
- muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12
- muscular dystrophy-dystroglycanopathy type B5
- muscular dystrophy-dystroglycanopathy type B6
- muscular dystrophy-dystroglycanopathy, type A
- muscular dystrophy-dystroglycanopathy, type B
- muscular dystrophy-dystroglycanopathy, type C
- muscular dystrophy-white matter spongiosis syndrome
- muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
- muscular pseudohypertrophy-hypothyroidism syndrome
- muscularis mucosa
- musculature
- musculature of body
- musculin
- musculo-skeletal system cell
- musculoskeletal embryonic nuclear protein 1
- musculoskeletal system
- musculoskeletal system benign neoplasm
- musculoskeletal system cancer
- musculoskeletal system disease
