long QT syndrome 10
long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3
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long QT syndrome 10
Summary
long QT syndrome 10 is a class of disease[1].
Key Facts
- long QT syndrome 10's instance of is recorded as class of disease[2].
- long QT syndrome 10's subclass of is recorded as long QT syndrome[3].
- long QT syndrome 10's subclass of is recorded as genetic disease[4].
- long QT syndrome 10's subclass of is recorded as autosomal dominant disease[5].
- long QT syndrome 10's MeSH descriptor ID is recorded as C567514[6].
- long QT syndrome 10's OMIM ID is recorded as 611819[7].
- long QT syndrome 10's Disease Ontology ID is recorded as DOID:0110651[8].
- long QT syndrome 10's health specialty is recorded as cardiology[9].
- long QT syndrome 10's genetic association is recorded as SCN4B[10].
- long QT syndrome 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110651[11].
- long QT syndrome 10's exact match is recorded as http://identifiers.org/doid/DOID:0110651[12].
- long QT syndrome 10's UMLS CUI is recorded as C2678484[13].
- long QT syndrome 10's ICD-10-CM is recorded as I45.8[14].
- long QT syndrome 10's GARD rare disease ID is recorded as 10436[15].
- long QT syndrome 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- long QT syndrome 10's Mondo ID is recorded as MONDO_0012737[17].
- long QT syndrome 10's UniProt disease ID is recorded as DI-00687[18].