Disease #00132 (LGMDR10 (MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 10), OMIM:608807)

Official abbreviation LGMDR10
Name MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 10
OMIM ID 608807
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TTN
Associated tissues -
Disease features -
Remarks -

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