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 2
Phenotype entries for this disease 1
Associated with 1 gene FLNC
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00269291 - - - - - Hong Kong;(Hong Kong) Chinese - - - - MFM5 - FLNC FLNC 1 34 Han-Chih Hencher Lee
00466089 338649 - - F no Germany - - - - - MFM5 Hypotonia, Muscle weakness, Peripheral neuropathy FLNC FLNC 1 1 Andreas Laner
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