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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00269291 - - - - - Hong Kong;(Hong Kong) Chinese - - - - MFM5 - FLNC FLNC 1 34 Han-Chih Hencher Lee
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