autosomal dominant limb-girdle muscular dystrophy type 1F
autosomal dominant limb-girdle muscular dystrophy that has material basis in heterozygous mutation in the TNPO3 gene on chromosome 7q32
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autosomal dominant limb-girdle muscular dystrophy type 1F
Summary
autosomal dominant limb-girdle muscular dystrophy type 1F is a rare disease[1].
Key Facts
- autosomal dominant limb-girdle muscular dystrophy type 1F's instance of is recorded as rare disease[2].
- autosomal dominant limb-girdle muscular dystrophy type 1F's instance of is recorded as class of disease[3].
- autosomal dominant limb-girdle muscular dystrophy type 1F's subclass of is recorded as autosomal dominant limb-girdle muscular dystrophy[4].
- autosomal dominant limb-girdle muscular dystrophy type 1F's MeSH descriptor ID is recorded as C564242[5].
- autosomal dominant limb-girdle muscular dystrophy type 1F's OMIM ID is recorded as 608423[6].
- autosomal dominant limb-girdle muscular dystrophy type 1F's Disease Ontology ID is recorded as DOID:0110304[7].
- autosomal dominant limb-girdle muscular dystrophy type 1F's Orphanet ID is recorded as 55595[8].
- autosomal dominant limb-girdle muscular dystrophy type 1F's health specialty is recorded as neurology[9].
- autosomal dominant limb-girdle muscular dystrophy type 1F's genetic association is recorded as TNPO3[10].
- autosomal dominant limb-girdle muscular dystrophy type 1F's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110304[11].
- autosomal dominant limb-girdle muscular dystrophy type 1F's exact match is recorded as http://identifiers.org/doid/DOID:0110304[12].
- autosomal dominant limb-girdle muscular dystrophy type 1F's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_55595[13].
- autosomal dominant limb-girdle muscular dystrophy type 1F's UMLS CUI is recorded as C1842062[14].
- autosomal dominant limb-girdle muscular dystrophy type 1F's ICD-10-CM is recorded as G71.0[15].
- autosomal dominant limb-girdle muscular dystrophy type 1F's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- autosomal dominant limb-girdle muscular dystrophy type 1F's Mondo ID is recorded as MONDO_0012034[17].
- autosomal dominant limb-girdle muscular dystrophy type 1F's UniProt disease ID is recorded as DI-04143[18].