Preferred Name |
long QT syndrome 1 |
|
Synonyms |
LQT1 |
|
Definitions |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4. |
|
ID |
http://purl.obolibrary.org/obo/DOID_0110644 |
|
database_cross_reference |
OMIM:192500 ICD10CM:I45.8 GARD:3284 |
|
definition |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4. |
|
has exact synonym |
LQT1 ventricular fibrillation with prolonged QT interval |
|
has material basis in | ||
has_obo_namespace |
disease_ontology |
|
id |
DOID:0110644 |
|
in_subset | ||
label |
long QT syndrome 1 |
|
notation |
DOID:0110644 |
|
prefLabel |
long QT syndrome 1 |
|
subClassOf |
http://purl.obolibrary.org/obo/DOID_0080578 |
Create mapping