Patent ductus arteriosus after birth at term
Symptom Information:
Symptom ID: | HPO:0011648 | ||||||||||||||
Synonyms: |
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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) Congenital malformation of the great arteries(HPO:0011603) Patent ductus arteriosus(HPO:0001643) Patent ductus arteriosus after birth at term(HPO:0011648) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Vascular malformations and acquired anomalies(MedDRA:10047091) Patent ductus arteriosus after birth at term(HPO:0011648) |
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Database Frequency: | 18 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
ADAMS-OLIVER SYNDROME 4 | (OMIM:615297) |
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA | (OMIM:613623) |
AORTIC ANEURYSM, FAMILIAL THORACIC 4 | (OMIM:132900) |
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Distal monosomy 10q | (Orphanet:96148) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome | (Orphanet:363611) |
Left ventricular noncompaction 1 | (OMIM:604169) |
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME | (OMIM:613834) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Nephronophthisis 16 | (OMIM:615382) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
VENTRICULAR SEPTAL DEFECT 3 | (OMIM:614432) |