Complete atrioventricular canal defect
Symptom Information:
Symptom ID: | HPO:0001674 | ||||||||||||||||||
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) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of the cardiac septa(HPO:0001671) Atrioventricular canal defect(HPO:0006695) Complete atrioventricular canal defect(HPO:0001674) MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) Myocardial disorders NEC(MedDRA:10028590) Complete atrioventricular canal defect(HPO:0001674) |
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Database Frequency: | 11 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ATRIAL SEPTAL DEFECT 2 | (OMIM:607941) |
ATRIOVENTRICULAR SEPTAL DEFECT 3 | (OMIM:600309) |
Conotruncal heart malformations | (Orphanet:2445) |
Diabetic embryopathy | (Orphanet:1926) |
Distal monosomy 3p | (Orphanet:1620) |
Down syndrome | (Orphanet:870) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
Heart defect - tongue hamartoma - polysyndactyly | (Orphanet:1338) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hydrolethalus | (Orphanet:2189) |
Ivemark syndrome | (Orphanet:97548) |