long QT syndrome 13
long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNJ5 gene on chromosome 11q24.3
Press Enter · cited answer in seconds
0 sources
long QT syndrome 13
Summary
long QT syndrome 13 is a rare disease[1].
Key Facts
- long QT syndrome 13's instance of is recorded as rare disease[2].
- long QT syndrome 13's instance of is recorded as class of disease[3].
- long QT syndrome 13's subclass of is recorded as long QT syndrome[4].
- long QT syndrome 13's subclass of is recorded as genetic disease[5].
- long QT syndrome 13's subclass of is recorded as autosomal dominant disease[6].
- long QT syndrome 13's OMIM ID is recorded as 613485[7].
- long QT syndrome 13's Disease Ontology ID is recorded as DOID:0110654[8].
- long QT syndrome 13's health specialty is recorded as cardiology[9].
- long QT syndrome 13's genetic association is recorded as KCNJ5[10].
- long QT syndrome 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110654[11].
- long QT syndrome 13's exact match is recorded as http://identifiers.org/doid/DOID:0110654[12].
- long QT syndrome 13's UMLS CUI is recorded as C3150733[13].
- long QT syndrome 13's ICD-10-CM is recorded as I45.8[14].
- long QT syndrome 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- long QT syndrome 13's Mondo ID is recorded as MONDO_0013279[16].
- long QT syndrome 13's UniProt disease ID is recorded as DI-02771[17].