Patent ductus arteriosus after birth at term

Symptom Information:

Symptom ID: HPO:0011648
Synonyms:
Patent ductus arteriosus [Orphanet:34520]
Patent ductus arteriosus (disorder) [Orphanet:34520]
Patent ductus arteriosus [MedDRA:10034130]
Ductus arteriosus patent [MedDRA:10034130]
Patent ductus arteriosis [MedDRA:10034130]
PDA [MedDRA:10034130]
Patent ductus arteriosis [OMIM:Patent ductus arteriosis]
Patent ductus arteriosus (1 patient) [OMIM:Patent ductus arteriosus (1 patient)]
Patent ductus arteriosus (2 patients) [OMIM:Patent ductus arteriosus (2 patients)]
Patent ductus arteriosus (in 1 reported case) [OMIM:Patent ductus arteriosus (in 1 reported case)]
Patent ductus arteriosus (in some patients) [OMIM:Patent ductus arteriosus (in some patients)]
Patent ductus arteriosus (less common) [OMIM:Patent ductus arteriosus (less common)]
Patent ductus arteriosus (male) [OMIM:Patent ductus arteriosus (male)]
Patent ductus arteriosus (rare) [OMIM:Patent ductus arteriosus (rare)]
Quality:
Cross references:
HPO:0001643 "Patent ductus arteriosus" [Orphanet:34520]
Orphanet:34520 "Patent ductus arteriosus" [Orphanet:34520]
OMIM: "Patent ductus arteriosis" [OMIM:Patent ductus arteriosis]
OMIM: "Patent ductus arteriosus (1 patient)" [OMIM:Patent ductus arteriosus (1 patient)]
OMIM: "Patent ductus arteriosus (2 patients)" [OMIM:Patent ductus arteriosus (2 patients)]
OMIM: "Patent ductus arteriosus (in 1 reported case)" [OMIM:Patent ductus arteriosus (in 1 reported case)]
OMIM: "Patent ductus arteriosus (in some patients)" [OMIM:Patent ductus arteriosus (in some patients)]
OMIM: "Patent ductus arteriosus (less common)" [OMIM:Patent ductus arteriosus (less common)]
OMIM: "Patent ductus arteriosus (male)" [OMIM:Patent ductus arteriosus (male)]
OMIM: "Patent ductus arteriosus (rare)" [OMIM:Patent ductus arteriosus (rare)]
UMLS:C0013274 "Patent ductus arteriosus" [Orphanet:34520]
Is a (Direct Parents):
HPO         Patent ductus arteriosus
MedDRA Vascular malformations and acquired anomalies
Orphanet obsolete Malformation of the heart and great vessels
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)
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)