Disease #00279 (MDDGA-7 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A7 (MDDGA-7)), OMIM:614643)
| Official abbreviation |
MDDGA-7 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A7 (MDDGA-7) |
| OMIM ID |
614643 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ISPD |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-11-22 17:27:42 +01:00 (CET) |
| Date last edited |
N/A |
|
