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

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00301615 - - heterozygous patient, family history M - Greece - 49y - - - MFM3;LGMD1A mother with acute ischemic stroke, son with cardiac defibrillator MYOT MYOT 1 1 Helen Latsoudis
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