Disease #03887 (MDDGA-13 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A13 (MDDGA-13)), OMIM:615287)
| Official abbreviation |
MDDGA-13 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A13 (MDDGA-13) |
| OMIM ID |
615287 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
B3GNT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
