RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL

General Information (adopted from Orphanet):

Synonyms, Signs: ARPA, FAMILIAL
RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, WITH VENTRICULAR SEPTAL DEFECT, PATENT FORAMEN OVALE, AND PATENT DUCTUS ARTERIOSUS
Number of Symptoms 8
OrphanetNr:
OMIM Id: 610338
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0005143) Anomalous origin of right pulmonary artery from ascending aorta 1 / 7739
2
(HPO:0001680) Coarctation of aorta 57 / 7739
3
(HPO:0001643) Patent ductus arteriosus 228 / 7739
4
(HPO:0001655) Patent foramen ovale 31 / 7739
5
(HPO:0001629) Ventricular septal defect 316 / 7739
6
(HPO:0001631) Atria septal defect 274 / 7739
7
(OMIM) Right pulmonary artery, anomalous origin of 1 / 7739
8
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Vergara et al. (2006) reported a 10-day-old male infant in whom echocardiography showed anomalous origin of the right pulmonary artery (ARPA) from the ascending aorta, patent foramen ovale, a small subaortic ventricular septal defect, and patent ductus arteriosus. ...