Mondo Disease Ontology
3933 terms(s) returned
| Term Type: | Record: 3501 to 3550 of 3933 Records | Page: 71 of 79, First Previous Next Last | Show Records Per Page |
- muscular dystrophy with reduced β-sarcoglycan, domestic cat
- muscular dystrophy, ANO5-related, rabbit
- muscular dystrophy, American mink
- muscular dystrophy, Barnes type
- muscular dystrophy, COL6A1-related, dog
- muscular dystrophy, COL6A3-related, dog
- muscular dystrophy, Duchenne type, dog
- muscular dystrophy, Duchenne type, domestic cat
- muscular dystrophy, Duchenne type, non-human animal
- muscular dystrophy, Duchenne type, pig
- muscular dystrophy, Hemizygous lethal type
- muscular dystrophy, Mabry type
- muscular dystrophy, TNNT1-related, sheep
- muscular dystrophy, adult-onset, with leukoencephalopathy
- muscular dystrophy, cardiac type
- muscular dystrophy, chicken
- muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome
- muscular dystrophy, congenital, with cerebellar atrophy
- 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, 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
