autosomal recessive limb-girdle muscular dystrophy

Summary

DOID:0110274 - autosomal recessive limb-girdle muscular dystrophy

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

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0015152 - autosomal recessive limb-girdle muscular dystrophy

MONDO:0015152 - autosomal recessive limb-girdle muscular dystrophy

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), limb-girdle muscular dystrophy (is_a)