Disease #04322 (VMCQA (myopathy, vacuolar, with CASQ1 aggregates (VMCQA)), OMIM:616231)
| Official abbreviation |
VMCQA |
| Name |
myopathy, vacuolar, with CASQ1 aggregates (VMCQA) |
| OMIM ID |
616231 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
8 |
| Associated with 1 gene |
CASQ1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-04 22:30:20 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|