| Metadata | |
|---|---|
| ID | DOID:0111240 |
| Name | congenital muscular dystrophy-dystroglycanopathy type A2 |
| Definition | A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in POMT2 on 14q24.3. https://www.ncbi.nlm.nih.gov/pubmed/15894594 |
| Xrefs | |
| Synonyms |
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2 [EXACT] MDDGA2 [EXACT] Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related [EXACT] |
| Parent Relationships |
is_a congenital muscular dystrophy-dystroglycanopathy type A |
| Subclass Logical Relationships |
disease has basis in some Abnormality of prenatal development or birth |