loading...| Preferred Name |
Romano-Ward syndrome |
|
| Synonyms |
Romano-Ward long QT syndrome |
|
| Definitions |
A form of familial long QT syndrome (LQTS) characterized by syncopal episodes and electrocardiographic abnormalities (QT prolongation, T-wave abnormalities and torsade de pointes (TdP) ventricular tachycardia). |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_101016 |
|
| alternative_term |
Romano-Ward long QT syndrome |
|
| definition |
A form of familial long QT syndrome (LQTS) characterized by syncopal episodes and electrocardiographic abnormalities (QT prolongation, T-wave abnormalities and torsade de pointes (TdP) ventricular tachycardia). |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=101016 |
|
| has_age_of_onset |
All ages |
|
| has_inheritance |
Autosomal recessive Autosomal dominant |
|
| hasDbXref |
OMIM:600919 OMIM:613485 OMIM:603830 OMIM:612955 OMIM:192500 ICD-10:I45.8 OMIM:611820 OMIM:616247 OMIM:616249 MedDRA:10039211 ICD-11:BC65.0 MeSH:D029597 OMIM:613693 OMIM:613695 UMLS:C4551647 OMIM:613688 OMIM:611819 OMIM:611818 |
|
| label |
Romano-Ward syndrome |
|
| notation |
ORPHA:101016 |
|
| part_of | ||
| prefixIRI |
ORDO:Orphanet_101016 |
|
| prefLabel |
Romano-Ward syndrome |
|
| present_in |
Europe AND has_point_prevalence_average_value : 40.0 AND has_point_prevalence_range : 1-5 / 10 000 |
|
| treeView | ||
| subClassOf |