Interrupted aortic arch

Symptom Information:

Symptom ID: HPO:0011611
Synonyms:
Atretic transverse aortic arch [HPO:0011611]
Aortic arch interruption [Orphanet:34320]
Interrupted aortic arch (disorder) [Orphanet:34320]
Interrupted aortic arch [Orphanet:34320]
Interrupted aortic arch [OMIM:Interrupted aortic arch]
Hypoplastic aorta/coarctation/stenosis/anomaly/aortic arch interruption [Orphanet:34320]
Interruption of aortic arch [Orphanet:34320]
Interruption of aortic arch [MedDRA:10022599]
Interrupted aortic arch (male) [OMIM:Interrupted aortic arch (male)]
Aorta hypoplasia [MedDRA:10049209]
Congenital hypoplasia of aorta (disorder) [Orphanet:34320]
Hypoplasia of aorta (disorder) [Orphanet:34320]
Hypoplasia of aorta [Orphanet:34320]
Quality:
Cross references:
Orphanet:34320 "Hypoplastic aorta/coarctation/stenosis/anomaly/aortic arch interruption" [Orphanet:34320]
OMIM: "Interrupted aortic arch" [OMIM:Interrupted aortic arch]
OMIM: "Interrupted aortic arch (male)" [OMIM:Interrupted aortic arch (male)]
UMLS:C0152419 "Interrupted aortic arch" [Orphanet:34320]
UMLS:C0265892 "Hypoplasia of aorta" [Orphanet:34320]
Is a (Direct Parents):
Orphanet obsolete Malformation of the heart and great vessels
Orphanet Coarctation of aorta
MedDRA Vascular malformations and acquired anomalies
HPO         Abnormality 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)
                      Interrupted aortic arch(HPO:0011611)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Interrupted aortic arch(HPO:0011611)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA (OMIM:107550)
Buschke-Ollendorff syndrome (Orphanet:1306)
DIGEORGE SYNDROME (OMIM:188400)
Diabetic embryopathy (Orphanet:1926)
Hypoplastic left heart syndrome (Orphanet:2248)
Hypoplastic left heart syndrome 2 (OMIM:614435)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Perlman syndrome (Orphanet:2849)