Right aortic arch

Symptom Information:

Symptom ID: HPO:0012020
Synonyms:
Right-sided aortic arch [HPO:0012020]
Right aortic arch [OMIM:Right aortic arch]
Right-sided aortic arch [OMIM:Right-sided aortic arch]
Right aortic arch (rare) [OMIM:Right aortic arch (rare)]
Right aortic arch [MedDRA:10067407]
Quality:
Cross references:
OMIM: "Right aortic arch" [OMIM:Right aortic arch]
OMIM: "Right-sided aortic arch" [OMIM:Right-sided aortic arch]
OMIM: "Right aortic arch (rare)" [OMIM:Right aortic arch (rare)]
Is a (Direct Parents):
MedDRA Vascular malformations and acquired anomalies
HPO         Abnormal branching pattern of the aortic arch
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormality of the aorta(HPO:0001679)
                   Abnormality of the aortic arch(HPO:0012303)
                      Abnormal branching pattern of the aortic arch(HPO:0011587)
                         Right aortic arch(HPO:0012020)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Right aortic arch(HPO:0012020)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2 (OMIM:606217)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
DIGEORGE SYNDROME (OMIM:188400)
Genito-palato-cardiac syndrome (Orphanet:2075)
HETEROTAXY, VISCERAL, 4, AUTOSOMAL (OMIM:613751)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)