autosomal dominant limb-girdle muscular dystrophy
limb-girdle muscular dystrophy that has material basis in autosomal dominant inheritance
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autosomal dominant limb-girdle muscular dystrophy
Summary
autosomal dominant limb-girdle muscular dystrophy is a rare disease[1].
Key Facts
- autosomal dominant limb-girdle muscular dystrophy's instance of is recorded as rare disease[2].
- autosomal dominant limb-girdle muscular dystrophy's instance of is recorded as class of disease[3].
- autosomal dominant limb-girdle muscular dystrophy's subclass of is recorded as limb-girdle muscular dystrophy[4].
- autosomal dominant limb-girdle muscular dystrophy's subclass of is recorded as autosomal dominant disease[5].
- autosomal dominant limb-girdle muscular dystrophy's Disease Ontology ID is recorded as DOID:0110273[6].
- autosomal dominant limb-girdle muscular dystrophy's Orphanet ID is recorded as 102014[7].
- autosomal dominant limb-girdle muscular dystrophy's health specialty is recorded as neurology[8].
- autosomal dominant limb-girdle muscular dystrophy's genetic association is recorded as MYOT[9].
- autosomal dominant limb-girdle muscular dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110273[10].
- autosomal dominant limb-girdle muscular dystrophy's exact match is recorded as http://identifiers.org/doid/DOID:0110273[11].
- autosomal dominant limb-girdle muscular dystrophy's UMLS CUI is recorded as C5675009[12].
- autosomal dominant limb-girdle muscular dystrophy's ICD-10-CM is recorded as G71.0[13].
- autosomal dominant limb-girdle muscular dystrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant limb-girdle muscular dystrophy's Mondo ID is recorded as MONDO_0015151[15].
- autosomal dominant limb-girdle muscular dystrophy's ICD-11 ID is recorded as 8C70.40[16].
- autosomal dominant limb-girdle muscular dystrophy's ICD-11 ID is recorded as 537908479[17].