autosomal dominant limb-girdle muscular dystrophy type 1G

Summary

autosomal dominant limb-girdle muscular dystrophy type 1G is a rare disease^[1].

Key Facts

• autosomal dominant limb-girdle muscular dystrophy type 1G's instance of is recorded as rare disease^[2].
• autosomal dominant limb-girdle muscular dystrophy type 1G's instance of is recorded as class of disease^[3].
• autosomal dominant limb-girdle muscular dystrophy type 1G's subclass of is recorded as autosomal dominant limb-girdle muscular dystrophy^[4].
• autosomal dominant limb-girdle muscular dystrophy type 1G's MeSH descriptor ID is recorded as C563794^[5].
• autosomal dominant limb-girdle muscular dystrophy type 1G's OMIM ID is recorded as 609115^[6].
• autosomal dominant limb-girdle muscular dystrophy type 1G's Disease Ontology ID is recorded as DOID:0110306^[7].
• autosomal dominant limb-girdle muscular dystrophy type 1G's Orphanet ID is recorded as 55596^[8].
• autosomal dominant limb-girdle muscular dystrophy type 1G's health specialty is recorded as neurology^[9].
• autosomal dominant limb-girdle muscular dystrophy type 1G's genetic association is recorded as HNRNPDL^[10].
• autosomal dominant limb-girdle muscular dystrophy type 1G's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110306^[11].
• autosomal dominant limb-girdle muscular dystrophy type 1G's exact match is recorded as http://identifiers.org/doid/DOID:0110306^[12].
• autosomal dominant limb-girdle muscular dystrophy type 1G's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_55596^[13].
• autosomal dominant limb-girdle muscular dystrophy type 1G's UMLS CUI is recorded as C1836765^[14].
• autosomal dominant limb-girdle muscular dystrophy type 1G's ICD-10-CM is recorded as G71.0^[15].
• autosomal dominant limb-girdle muscular dystrophy type 1G's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].
• autosomal dominant limb-girdle muscular dystrophy type 1G's Mondo ID is recorded as MONDO_0012193^[17].