Disease #01449 (MFM3;LGMD1A (myopathy, myofibrillar, type 3 (LGMD1A)), OMIM:159000)

Official abbreviation MFM3;LGMD1A
Name myopathy, myofibrillar, type 3 (LGMD1A)
OMIM ID 159000
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 2024-01-12 20:44:04 +01:00 (CET)


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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