Disease #06201 (CMYO16;MYOTREM (myopathy, congenital, type 16), OMIM:618524)
| Official abbreviation |
CMYO16;MYOTREM |
| Name |
myopathy, congenital, type 16 |
| OMIM ID |
618524 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MYBPC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2026-02-06 10:11:07 +01:00 (CET) |
Individuals
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