Disease #05713 (MYOCOZ (myopathy, congenital with structured cores and Z-line abnormalitie (MYOCOZ)), OMIM:618654)
| Official abbreviation |
MYOCOZ |
| Name |
myopathy, congenital with structured cores and Z-line abnormalitie (MYOCOZ) |
| OMIM ID |
618654 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ACTN2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-03-29 14:08:06 +02:00 (CEST) |
| Date last edited |
2020-05-03 14:14:32 +02:00 (CEST) |
Individuals
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