Jump to:
loading...| 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 OMIM:613688 GARD:3285 |
|
| 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 |
Create mapping