autosomal recessive limb-girdle muscular dystrophy type 2C
autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12
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autosomal recessive limb-girdle muscular dystrophy type 2C
Summary
autosomal recessive limb-girdle muscular dystrophy type 2C is a class of disease[1].
Key Facts
- autosomal recessive limb-girdle muscular dystrophy type 2C's instance of is recorded as class of disease[2].
- autosomal recessive limb-girdle muscular dystrophy type 2C is a type of autosomal recessive limb-girdle muscular dystrophy[3].
- autosomal recessive limb-girdle muscular dystrophy type 2C is a type of sarcoglycanopathy[4].
- autosomal recessive limb-girdle muscular dystrophy type 2C is a type of qualitative or quantitative defects of gamma-sarcoglycan[5].
- autosomal recessive limb-girdle muscular dystrophy type 2C is a type of neuromuscular disease with dilated cardiomyopathy[6].
- autosomal recessive limb-girdle muscular dystrophy type 2C's health specialty is recorded as neurology[7].
- autosomal recessive limb-girdle muscular dystrophy type 2C's genetic association is recorded as SGCG[8].
- autosomal recessive limb-girdle muscular dystrophy type 2C's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110277[9].
- autosomal recessive limb-girdle muscular dystrophy type 2C's exact match is recorded as http://identifiers.org/doid/DOID:0110277[10].
- autosomal recessive limb-girdle muscular dystrophy type 2C's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].