Disease #01449 (LGMD-1A (dystrophy, muscular, limb-girdle, type 1A (LGMD-1A)), OMIM:159000)

Official abbreviation LGMD-1A
Name dystrophy, muscular, limb-girdle, type 1A (LGMD-1A)
OMIM ID 159000
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MYOT
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Individuals

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00301615 - - heterozygous patient, family history M - Greece - 49y 0 - - LGMD-1A mother with acute ischemic stroke, son with cardiac defibrillator MYOT MYOT 1 1 Helen Latsoudis
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