congenital structural myopathy
human disease
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congenital structural myopathy
Summary
congenital structural myopathy is a class of disease[1].
Key Facts
- congenital structural myopathy's instance of is recorded as class of disease[2].
- congenital structural myopathy's subclass of is recorded as muscular disease[3].
- congenital structural myopathy's MeSH descriptor ID is recorded as D020914[4].
- congenital structural myopathy's MeSH tree code is recorded as C05.651.575[5].
- congenital structural myopathy's MeSH tree code is recorded as C10.668.491.550[6].
- congenital structural myopathy's Disease Ontology ID is recorded as DOID:422[7].
- congenital structural myopathy's NCI Thesaurus ID is recorded as C84648[8].
- congenital structural myopathy's health specialty is recorded as neurology[9].
- congenital structural myopathy's health specialty is recorded as rheumatology[10].
- congenital structural myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_422[11].
- congenital structural myopathy's exact match is recorded as http://identifiers.org/doid/DOID:422[12].
- congenital structural myopathy's UMLS CUI is recorded as C0752282[13].
- congenital structural myopathy's UMLS CUI is recorded as C0546264[14].
- congenital structural myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].