Mondo Disease Ontology
4242 terms(s) returned
| Term Type: | Record: 3801 to 3850 of 4242 Records | Page: 77 of 85, First Previous Next Last | Show Records Per Page |
- muscular dystrophy, congenital, with or without seizures
- muscular dystrophy, congenital, with rapid progression
- muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers
- muscular dystrophy, dog
- muscular dystrophy, domestic cat
- muscular dystrophy, goat
- 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 26
- muscular dystrophy, limb-girdle, autosomal recessive 27
- muscular dystrophy, limb-girdle, autosomal recessive 28
- muscular dystrophy, limb-girdle, autosomal recessive 29
- muscular dystrophy, non-human animal
- muscular dystrophy, progressive Pectorodorsal
- muscular dystrophy, pseudohypertrophic, with Internalized capillaries
- muscular dystrophy, scapulohumeral
- muscular dystrophy, sheep
- muscular dystrophy, turkey
- 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), COLQ-related, domestic cat
- muscular dystrophy-dystroglycanopathy (limb-girdle), chicken
- muscular dystrophy-dystroglycanopathy (limb-girdle), non-human animal
- muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
- muscular dystrophy-dystroglycanopathy type B5
- muscular dystrophy-dystroglycanopathy type B6
- muscular dystrophy-dystroglycanopathy, LARGE1-related, dog
- muscular dystrophy-dystroglycanopathy, type A
- muscular dystrophy-dystroglycanopathy, type B
- muscular dystrophy-dystroglycanopathy, type C
