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
|