Congenital Muscular Dystrophy-Dystroglycanopathy Type A10
Disease ID: disease_node_17419
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| Dbxref | MIM:615041 |
|---|---|
| Subclassof | DOID_0111229 |
| Data Source | DOID |
| Synonyms | MDDGA10, Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related, congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10 |
| Doid Label | congenital muscular dystrophy-dystroglycanopathy type A10 |
| Doid Description | A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2. |
| Disease Node Id | disease_node_17419 |
| Doid Id | DOID_0111239 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Muscular Dystrophy-Dystroglycanopathy Type A10 |
- Outgoing r'ship
SUBCLASS_OFto/from Congenital Muscular Dystrophy-Dystroglycanopathy Type A(ID:disease_node_17406) (Disease)