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Echinobase
Summary Literature (0)
DOID:0110293 - autosomal recessive limb-girdle muscular dystrophy type 2P

Disease Ontology Definition:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21.

Synonyms: LGMD2P, MDDGC9, muscular dystrophy-dystroglycanopathy (limb-girdle) type C9, muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related,

Echinobase Genes : dag1


OMIM:
MIM:613818 - muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9; mddgc9

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive limb-girdle muscular dystrophy (is_a)