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Summary Literature (0)
DOID:0110274 - autosomal recessive limb-girdle muscular dystrophy


Disease Ontology Definition:A limb-girdle muscular dystrophy has_material_basis_in autosomal recessive inheritance.

Synonyms:


In Mondo Disease Ontology:
MONDO:0015152 - autosomal recessive limb-girdle muscular dystrophy

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : bves, gmppb, sgcb, pomt1, sgcd, tor1aip1, sgcg, pomgnt1, fkrp, fktn, pomt2, trim32, tcap, crppa, dag1, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), limb-girdle muscular dystrophy (is_a)