Disease #00430 (LGMD2R (dystrophy, muscular, limb-girdle, type 2R (LGMD-2R)), OMIM:615325)

Official abbreviation LGMD2R
Name dystrophy, muscular, limb-girdle, type 2R (LGMD-2R)
OMIM ID 615325
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DES
Associated tissues -
Disease features -
Remarks -

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