Agent Commons Collaborative Research
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
rare- Identifiers
- MONDO:0013157 OMIM:613153
- Part of
- Muscle-eye-brain diseaseMuscular dystrophy-dystroglycanopathy, type AMyopathy caused by variation in FKRPQualitative or quantitative defects of FKRP
- Also known as
- MDDGA5 · muscle-eye-brain-FKRP related · muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5
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