reducing body myopathy

Summary

reducing body myopathy is a rare disease^[1].

Key Facts

• reducing body myopathy's instance of is recorded as rare disease^[2].
• reducing body myopathy's instance of is recorded as class of disease^[3].
• reducing body myopathy's subclass of is recorded as muscular disease^[4].
• reducing body myopathy's subclass of is recorded as X-linked dominant disease^[5].
• reducing body myopathy's MeSH descriptor ID is recorded as C567469^[6].
• reducing body myopathy's OMIM ID is recorded as 300718^[7].
• reducing body myopathy's OMIM ID is recorded as 300717^[8].
• reducing body myopathy's KEGG ID is recorded as H00657^[9].
• reducing body myopathy's Disease Ontology ID is recorded as DOID:0080090^[10].
• reducing body myopathy's genetic association is recorded as FHL1^[11].
• reducing body myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080090^[12].
• reducing body myopathy's exact match is recorded as http://identifiers.org/doid/DOID:0080090^[13].
• reducing body myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97239^[14].
• reducing body myopathy's UMLS CUI is recorded as C2678027^[15].
• reducing body myopathy's GARD rare disease ID is recorded as 12162^[16].
• reducing body myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• reducing body myopathy's Mondo ID is recorded as MONDO_0010414^[18].
• reducing body myopathy's UniProt disease ID is recorded as DI-02458^[19].