Disease #01107 (MDDGA-2;MEB;WWS (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A2 (MDDGA-2, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB))), OMIM:613150)
| Official abbreviation |
MDDGA-2;MEB;WWS |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A2 (MDDGA-2, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB)) |
| OMIM ID |
613150 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
POMT2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
