Disease #01100 (LGMD-2M;MDDGC-4 (dystrophy, muscular, limb-girdle, type 2M (LGMD-2M, dystroglycanopathy C4 (MDDGC-4))), OMIM:611588)
| Official abbreviation |
LGMD-2M;MDDGC-4 |
| Name |
dystrophy, muscular, limb-girdle, type 2M (LGMD-2M, dystroglycanopathy C4 (MDDGC-4)) |
| OMIM ID |
611588 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FKTN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
