Disease #02855 (MFM5 (myopathy, myofibrillar, type 5 (MFM-5, filamin C related)), OMIM:609524)
Official abbreviation |
MFM5 |
Name |
myopathy, myofibrillar, type 5 (MFM-5, filamin C related) |
OMIM ID |
609524 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
FLNC |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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