long QT syndrome 11
long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2
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Summary
long QT syndrome 11 is a rare disease[1].
Key Facts
- long QT syndrome 11's instance of is recorded as rare disease[2].
- long QT syndrome 11's instance of is recorded as class of disease[3].
- long QT syndrome 11's subclass of is recorded as long QT syndrome[4].
- long QT syndrome 11's subclass of is recorded as genetic disease[5].
- long QT syndrome 11's MeSH descriptor ID is recorded as C567513[6].
- long QT syndrome 11's OMIM ID is recorded as 611820[7].
- long QT syndrome 11's Disease Ontology ID is recorded as DOID:0110652[8].
- long QT syndrome 11's NCI Thesaurus ID is recorded as C192195[9].
- long QT syndrome 11's health specialty is recorded as cardiology[10].
- long QT syndrome 11's genetic association is recorded as AKAP9[11].
- long QT syndrome 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110652[12].
- long QT syndrome 11's exact match is recorded as http://identifiers.org/doid/DOID:0110652[13].
- long QT syndrome 11's UMLS CUI is recorded as C2678483[14].
- long QT syndrome 11's ICD-10-CM is recorded as I45.8[15].
- long QT syndrome 11's GARD rare disease ID is recorded as 10437[16].
- long QT syndrome 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- long QT syndrome 11's Mondo ID is recorded as MONDO_0012738[18].
- long QT syndrome 11's UniProt disease ID is recorded as DI-00688[19].