Disease #01102 (MDDGC1;LGMDR11;LGMD2K (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C1 (LGMDR11, LGMD2K)), OMIM:609308)
| Official abbreviation |
MDDGC1;LGMDR11;LGMD2K |
| Name |
dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C1 (LGMDR11, LGMD2K) |
| OMIM ID |
609308 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
POMT1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-01-12 21:49:34 +01:00 (CET) |
Individuals
|