autosomal recessive limb-girdle muscular dystrophy type 2F
autosomal recessive limb-girdle muscular dystrophy that has material basis in mutation in the sarcoglycan-delta gene (SGCD)
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autosomal recessive limb-girdle muscular dystrophy type 2F
Summary
autosomal recessive limb-girdle muscular dystrophy type 2F is a rare disease[1].
Key Facts
- autosomal recessive limb-girdle muscular dystrophy type 2F's instance of is recorded as rare disease[2].
- autosomal recessive limb-girdle muscular dystrophy type 2F's instance of is recorded as class of disease[3].
- autosomal recessive limb-girdle muscular dystrophy type 2F is a type of autosomal recessive limb-girdle muscular dystrophy[4].
- autosomal recessive limb-girdle muscular dystrophy type 2F is a type of sarcoglycanopathy[5].
- autosomal recessive limb-girdle muscular dystrophy type 2F is a type of qualitative or quantitative defects of delta-sarcoglycan[6].
- autosomal recessive limb-girdle muscular dystrophy type 2F is a type of neuromuscular disease with dilated cardiomyopathy[7].
- autosomal recessive limb-girdle muscular dystrophy type 2F's health specialty is recorded as neurology[8].
- autosomal recessive limb-girdle muscular dystrophy type 2F's health specialty is recorded as myology[9].
- autosomal recessive limb-girdle muscular dystrophy type 2F's genetic association is recorded as SGCD[10].
- autosomal recessive limb-girdle muscular dystrophy type 2F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110280[11].
- autosomal recessive limb-girdle muscular dystrophy type 2F's exact match is recorded as http://identifiers.org/doid/DOID:0110280[12].
- autosomal recessive limb-girdle muscular dystrophy type 2F's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].