Disease #01449 (MFM3;LGMD1A (myopathy, myofibrillar, type 3), OMIM:609200)
| Official abbreviation |
MFM3;LGMD1A |
| Name |
myopathy, myofibrillar, type 3 |
| OMIM ID |
609200 |
| 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 |
MYOT |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2026-04-09 15:41:30 +02:00 (CEST) |
Individuals
|