Truncus arteriosus

Symptom Information:

Symptom ID: HPO:0001660
Synonyms:
Common arterial trunk [HPO:0001660]
Persistant truncus arteriosus [HPO:0001660]
Common arterial trunk [Orphanet:34400]
Common truncus arteriosus (disorder) [Orphanet:34400]
Truncus Arteriosus, Persistent [Orphanet:34400]
Truncus arteriosus [OMIM:Truncus arteriosus]
Common arterial trunk/truncal valve [Orphanet:34400]
Truncus arteriosus persistent [Orphanet:34400]
Truncus arteriosus persistent [MedDRA:10044703]
Common truncus [MedDRA:10044703]
Truncus arteriosus communis [MedDRA:10044703]
Truncus arteriosus communis [OMIM:Truncus arteriosus communis]
Truncus arteriosus communis (rare) [OMIM:Truncus arteriosus communis (rare)]
Truncal valve [Orphanet:34400]
Quality:
Cross references:
Orphanet:34400 "Common arterial trunk/truncal valve" [Orphanet:34400]
OMIM: "Truncus arteriosus" [OMIM:Truncus arteriosus]
OMIM: "Truncus arteriosus communis" [OMIM:Truncus arteriosus communis]
OMIM: "Truncus arteriosus communis (rare)" [OMIM:Truncus arteriosus communis (rare)]
UMLS:C0041207 "Truncus Arteriosus, Persistent" [Orphanet:34400]
Is a (Direct Parents):
Orphanet obsolete Malformation of the heart and great vessels
MedDRA Vascular malformations and acquired anomalies
HPO         Congenital malformation of the great arteries
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)
                   Truncus arteriosus(HPO:0001660)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Truncus arteriosus(HPO:0001660)
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 deletion syndrome (Orphanet:567)
Acro-cardio-facial syndrome (Orphanet:2008)
Conotruncal heart malformations (Orphanet:2445)
DIGEORGE SYNDROME (OMIM:188400)
Diabetic embryopathy (Orphanet:1926)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Double outlet right ventricle (Orphanet:3426)
Emanuel syndrome (Orphanet:96170)
Femoral-facial syndrome (Orphanet:1988)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Hypoplastic left heart syndrome 2 (OMIM:614435)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Matthew-Wood syndrome (Orphanet:2470)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microgastria - limb reduction defect (Orphanet:2538)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 (OMIM:615415)
THYMIC APLASIA WITH FETAL DEATH (OMIM:274210)
Truncus arteriosus (Orphanet:3384)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)