long QT syndrome 12
long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21
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Summary
long QT syndrome 12 is a rare disease[1].
Key Facts
- long QT syndrome 12's instance of is recorded as rare disease[2].
- long QT syndrome 12's instance of is recorded as class of disease[3].
- long QT syndrome 12's subclass of is recorded as long QT syndrome[4].
- long QT syndrome 12's subclass of is recorded as genetic disease[5].
- long QT syndrome 12's MeSH descriptor ID is recorded as C567842[6].
- long QT syndrome 12's OMIM ID is recorded as 612955[7].
- long QT syndrome 12's Disease Ontology ID is recorded as DOID:0110653[8].
- long QT syndrome 12's NCI Thesaurus ID is recorded as C192202[9].
- long QT syndrome 12's health specialty is recorded as cardiology[10].
- long QT syndrome 12's genetic association is recorded as SNTA1[11].
- long QT syndrome 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110653[12].
- long QT syndrome 12's exact match is recorded as http://identifiers.org/doid/DOID:0110653[13].
- long QT syndrome 12's UMLS CUI is recorded as C2751830[14].
- long QT syndrome 12's ICD-10-CM is recorded as I45.8[15].
- long QT syndrome 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- long QT syndrome 12's Mondo ID is recorded as MONDO_0013062[17].
- long QT syndrome 12's UniProt disease ID is recorded as DI-02487[18].