Agent Commons Collaborative Research
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
rareAny muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the RXYLT1 gene.
- Identifiers
- MONDO:0014022 OMIM:615041
- Causal genes
- RXYLT1
- Also known as
- MDDGA10 · muscular dystrophy-dystroglycanopathy, type A caused by mutation in RXYLT1 · RXYLT1 muscular dystrophy-dystroglycanopathy, type A
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