Disease

congenital muscular dystrophy due to integrin alpha-7 deficiency

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 integrin alpha-7 deficiency
congenital muscular dystrophy with ITGA7 deficiency

Cross References

Parent Terms

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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