Disease #06727 (LGMDR26 (dystrophy, muscular, limb-girdle, autosomal recessive, type 26), OMIM:618848)
| Official abbreviation |
LGMDR26 |
| Name |
dystrophy, muscular, limb-girdle, autosomal recessive, type 26 |
| OMIM ID |
618848 |
| 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 |
POPDC3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2024-01-10 22:25:07 +01:00 (CET) |
Individuals
|