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loading...| Preferred Name |
long QT syndrome 5 |
| Synonyms |
LQT5 |
| Definitions |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE1 gene on chromosome 21q22.12. |
| ID |
http://purl.obolibrary.org/obo/DOID_0110647 |
| database_cross_reference |
MESH:C566766 OMIM:613695 ICD10CM:I45.8 GARD:10433 |
| definition |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE1 gene on chromosome 21q22.12. |
| has exact synonym |
LQT5 |
| has material basis in | |
| has_obo_namespace |
disease_ontology |
| id |
DOID:0110647 |
| in_subset | |
| label |
long QT syndrome 5 |
| notation |
DOID:0110647 |
| prefLabel |
long QT syndrome 5 |
| subClassOf |
http://purl.obolibrary.org/obo/DOID_2843 |
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