Interrupted aortic arch
Symptom Information:
Symptom ID: | HPO:0011611 | |||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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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) |