autosomal recessive limb-girdle muscular dystrophy type R1
autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15
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autosomal recessive limb-girdle muscular dystrophy type R1
Summary
autosomal recessive limb-girdle muscular dystrophy type R1 is a rare disease[1]. It draws 6 Wikipedia views per month (rare_disease category, ranking #225 of 627).[2]
Key Facts
- autosomal recessive limb-girdle muscular dystrophy type R1's instance of is recorded as rare disease[3].
- autosomal recessive limb-girdle muscular dystrophy type R1's instance of is recorded as class of disease[4].
- autosomal recessive limb-girdle muscular dystrophy type R1 is a type of autosomal recessive limb-girdle muscular dystrophy[5].
- autosomal recessive limb-girdle muscular dystrophy type R1 is a type of disease[6].
- autosomal recessive limb-girdle muscular dystrophy type R1's Commons category is recorded as Calpainopathy[7].
- autosomal recessive limb-girdle muscular dystrophy type R1's NCI Thesaurus ID is recorded as C142079[8].
- autosomal recessive limb-girdle muscular dystrophy type R1's health specialty is recorded as neurology[9].
- autosomal recessive limb-girdle muscular dystrophy type R1's health specialty is recorded as myology[10].
- autosomal recessive limb-girdle muscular dystrophy type R1's genetic association is recorded as CAPN3[11].
- autosomal recessive limb-girdle muscular dystrophy type R1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110275[12].
- autosomal recessive limb-girdle muscular dystrophy type R1's exact match is recorded as http://identifiers.org/doid/DOID:0110275[13].
- autosomal recessive limb-girdle muscular dystrophy type R1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_267[14].
- autosomal recessive limb-girdle muscular dystrophy type R1's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
autosomal recessive limb-girdle muscular dystrophy type R1 draws 6 Wikipedia views per month (rare_disease category, ranking #225 of 627).[2] It is known by 13 alternative names across languages and contexts.[16]