congenital muscular dystrophy due to integrin alpha-7 deficiency
congenital muscular dystrophy characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the ITGA7 gene on chromosome 12q13
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congenital muscular dystrophy due to integrin alpha-7 deficiency
Summary
congenital muscular dystrophy due to integrin alpha-7 deficiency is a rare disease[1].
Key Facts
- congenital muscular dystrophy due to integrin alpha-7 deficiency's instance of is recorded as rare disease[2].
- congenital muscular dystrophy due to integrin alpha-7 deficiency's instance of is recorded as class of disease[3].
- congenital muscular dystrophy due to integrin alpha-7 deficiency is a type of congenital muscular dystrophy[4].
- congenital muscular dystrophy due to integrin alpha-7 deficiency is a type of qualitative or quantitative defects of integrin alpha-7[5].
- congenital muscular dystrophy due to integrin alpha-7 deficiency is a type of genetic disease[6].
- congenital muscular dystrophy due to integrin alpha-7 deficiency is a type of autosomal recessive disease[7].
- congenital muscular dystrophy due to integrin alpha-7 deficiency's health specialty is recorded as neurology[8].
- congenital muscular dystrophy due to integrin alpha-7 deficiency's genetic association is recorded as ITGA7[9].
- congenital muscular dystrophy due to integrin alpha-7 deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110639[10].
- congenital muscular dystrophy due to integrin alpha-7 deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0110639[11].
- congenital muscular dystrophy due to integrin alpha-7 deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].