Disease #00005 (LGMD-2I;MDDGC-5 (dystrophy, muscular, limb-girdle, type 2I (LGMD-2I, dystroglycanopathy C5 (MDDGC-5))), OMIM:607155)
| Official abbreviation |
LGMD-2I;MDDGC-5 |
| Name |
dystrophy, muscular, limb-girdle, type 2I (LGMD-2I, dystroglycanopathy C5 (MDDGC-5)) |
| OMIM ID |
607155 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FKRP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-06-11 11:22:53 +02:00 (CEST) |
| Date last edited |
N/A |
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