Mondo Disease Ontology
3949 terms(s) returned
| Term Type: | Record: 3551 to 3600 of 3949 Records | Page: 72 of 79, First Previous Next Last | Show Records Per Page |
- 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), chicken
- muscular dystrophy-dystroglycanopathy (limb-girdle), domestic cat
- 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
- muscular dystrophy-white matter spongiosis syndrome
- muscular fibrosis multifocal obstructed vessels
- muscular hypertonia, lethal
- muscular hypertrophy, MSTN-related, cattle
- 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
- musculature of forelimb stylopod
- musculature of forelimb zeugopod
- musculature of hindlimb stylopod
