congenital muscular dystrophy-dystroglycanopathy type A9 (Q66084928)
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A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.
- congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
- Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
- MDDGA9
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital muscular dystrophy-dystroglycanopathy type A9 |
A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in DAG1 on 3p21.31. |
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Identifiers
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1 reference