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Summary Literature (0)
DOID:0110639 - congenital muscular dystrophy due to integrin alpha-7 deficiency

Disease Ontology Definition:A congenital muscular dystrophy characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13.

Synonyms: congenital muscular dystrophy with ITGA7 deficiency, congenital muscular dystrophy with integrin alpha-7 deficiency, congenital myopathy due to integrin alpha-7 deficiency ,

Xenbase Genes : itga7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013177 - congenital muscular dystrophy due to integrin alpha-7 deficiency


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), congenital muscular dystrophy (is_a)