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congenital muscular dystrophy due to integrin alpha-7 deficiency (DOID:0110639)
Alliance: disease page
Synonyms: congenital muscular dystrophy with integrin alpha-7 deficiency; congenital muscular dystrophy with ITGA7 deficiency; congenital myopathy due to integrin alpha-7 deficiency
Alt IDs: OMIM:613204, ICD10CM:G71.2, ORDO:34520
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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.21
The Jackson Laboratory