Disease #04526 (MDDGC-7 (dystrophy, muscular, dystroglycanopathy, type C7 (MDDGC-7, limb-girdle)), OMIM:616052)
| Official abbreviation |
MDDGC-7 |
| Name |
dystrophy, muscular, dystroglycanopathy, type C7 (MDDGC-7, limb-girdle) |
| OMIM ID |
616052 |
| 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 |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
N/A |
|
|
