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Human Health Exposure Analysis Resource
Last uploaded:
July 19, 2024
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| Preferred Name | long QT syndrome 2 | |
| Synonyms |
LQT2 |
|
| Definitions |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0110645 |
|
| alternative label |
LQT2
|
|
| database_cross_reference |
ICD10CM:I45.8 MESH:C563614 GARD:3285 MIM:613688
|
|
| definition |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.
|
|
| has exact synonym |
LQT2
|
|
| has material basis in | ||
| has_obo_namespace |
disease_ontology
|
|
| id |
DOID:0110645
|
|
| in_subset | ||
| label |
long QT syndrome 2
|
|
| notation |
DOID:0110645
|
|
| note |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.
|
|
| preferred label |
long QT syndrome 2
|
|
| prefLabel |
long QT syndrome 2
|
|
| subClassOf |
http://purl.obolibrary.org/obo/DOID_0080578 |
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