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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Double outlet right ventricle | |
| Synonyms |
DORV |
|
| Definitions |
A rare cono-truncal anomaly in which both the aorta and pulmonary artery originate, either entirely or predominantly, from the morphologic right ventricle. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_3426 |
|
| alternative_term |
DORV
|
|
| definition |
A rare cono-truncal anomaly in which both the aorta and pulmonary artery originate, either entirely or predominantly, from the morphologic right ventricle.
|
|
| definition_citation |
Orphanet
|
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=3426 |
|
| has_age_of_onset |
Infancy Neonatal
|
|
| has_inheritance |
Multigenic/multifactorial
|
|
| hasDbXref |
ICD-10:Q20.1 UMLS:C0013069 OMIM:217095 MedDRA:10013611 ICD-11:LA85.2 MeSH:D004310
|
|
| label |
Double outlet right ventricle
|
|
| notation |
ORPHA:3426
|
|
| part_of | ||
| prefixIRI |
ORDO:Orphanet_3426
|
|
| prefLabel |
Double outlet right ventricle
|
|
| present_in |
Germany AND has_birth_prevalence_average_value : 10.0 AND has_birth_prevalence_range : 1-5 / 10 000 Europe AND has_point_prevalence_range : 1-5 / 10 000
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| treeView | ||
| subClassOf |
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