Mondo Disease Ontology
3641 terms(s) returned
Term Type: Class | Record: 3251 to 3300 of 3641 Records | Page: 66 of 73, First Previous Next Last | Show Records Per Page |
- muscular dystrophy, limb-girdle, autosomal recessive 26
- muscular dystrophy, limb-girdle, autosomal recessive 27
- muscular dystrophy, limb-girdle, autosomal recessive 28
- 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), type C, 8
- 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 fibrosis multifocal obstructed vessels
- muscular hypertonia, lethal
- muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
- muscular hypoplasia, congenital universal, of Krabbe
- muscular layer of prostatic urethra
- muscular layer of vagina
- muscular pseudohypertrophy-hypothyroidism syndrome
- musculature
- musculature of arm
- musculature of back
- musculature of body
- musculature of body wall
- musculature of face