Disease #00073 (MDDGA-3;MEB;WWS (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A3 (MDDGA-3, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB))), OMIM:253280)
| Official abbreviation |
MDDGA-3;MEB;WWS |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A3 (MDDGA-3, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB)) |
| OMIM ID |
253280 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
POMGNT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-11-09 14:33:21 +01:00 (CET) |
| Date last edited |
N/A |
|
