Disease #00123 (MDDGA-1;MEB;WWS (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A1 (MDDGA-1, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB))), OMIM:236670)
| Official abbreviation |
MDDGA-1;MEB;WWS |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A1 (MDDGA-1, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB)) |
| OMIM ID |
236670 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
POMT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-05-01 14:12:40 +02:00 (CEST) |
| Date last edited |
N/A |
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