Transposition of the great arteries

Symptom Information:

Symptom ID: HPO:0001669
Synonyms:
Transposition of great vessels [HPO:0001669]
Transposition of great vessels [Orphanet:34360]
Complete transposition of great vessels (disorder) [Orphanet:34360]
Total great vessel transposition (disorder) [Orphanet:34360]
Discordant ventriculoarterial connection (disorder) [Orphanet:34360]
Transposition of Great Vessels [Orphanet:34360]
Transposition of great vessels [OMIM:Transposition of great vessels]
Transposition of the great arteries [OMIM:Transposition of the great arteries]
Transposition of the great vessels [Orphanet:34360]
Transposition of the great vessels [MedDRA:10044443]
Aorta-pulmonary art transposition [MedDRA:10044443]
Aorta-pulmonary arterial transposition [MedDRA:10044443]
Complete transposition of great vessels [MedDRA:10044443]
Other transposition of great vessels [MedDRA:10044443]
Transposition aorta-pulmonary artery [MedDRA:10044443]
Transposition of aorta [MedDRA:10044443]
Transposition of great vessels [MedDRA:10044443]
Transposition of great vessels (rare) [OMIM:Transposition of great vessels (rare)]
Transposition of the great vessels [OMIM:Transposition of the great vessels]
Quality:
Cross references:
Orphanet:34360 "Transposition of great vessels" [Orphanet:34360]
OMIM: "Transposition of great vessels" [OMIM:Transposition of great vessels]
OMIM: "Transposition of the great arteries" [OMIM:Transposition of the great arteries]
OMIM: "Transposition of great vessels (rare)" [OMIM:Transposition of great vessels (rare)]
OMIM: "Transposition of the great vessels" [OMIM:Transposition of the great vessels]
UMLS:C0040761 "Transposition of Great Vessels" [Orphanet:34360]
Is a (Direct Parents):
Orphanet obsolete Malformation of the heart and great vessels
HPO         Congenital malformation of the great arteries
HPO         Abnormal ventriculo-arterial connection
MedDRA Vascular malformations and acquired anomalies
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)
                   Transposition of the great arteries(HPO:0001669)
                Abnormal connection of the cardiac segments(HPO:0011545)
                   Abnormal ventriculo-arterial connection(HPO:0011563)
                      Transposition of the great arteries(HPO:0001669)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Transposition of the great arteries(HPO:0001669)
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

16p13.11 microduplication syndrome (Orphanet:261243)
1q21.1 microdeletion syndrome (Orphanet:250989)
22q11.2 microduplication syndrome (Orphanet:1727)
8p23.1 microdeletion syndrome (Orphanet:251071)
CARPENTER SYNDROME 1 (OMIM:201000)
CARPENTER SYNDROME 2 (OMIM:614976)
Cantrell pentalogy (Orphanet:1335)
Carpenter syndrome (Orphanet:65759)
Congenitally uncorrected transposition of the great arteries (Orphanet:860)
Conotruncal heart malformations (Orphanet:2445)
Criss-cross heart (Orphanet:1461)
Diabetic embryopathy (Orphanet:1926)
Double outlet right ventricle (Orphanet:3426)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS (OMIM:227255)
Familial caudal dysgenesis (Orphanet:1768)
Fetal trimethadione syndrome (Orphanet:1913)
Genito-palato-cardiac syndrome (Orphanet:2075)
HETEROTAXY, VISCERAL, 5, AUTOSOMAL (OMIM:270100)
HETEROTAXY, VISCERAL, 6, AUTOSOMAL (OMIM:614779)
Heterotaxia (Orphanet:450)
Kallmann syndrome - heart disease (Orphanet:2326)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
Meacham syndrome (Orphanet:3097)
Nephronophthisis 9 (OMIM:613824)
Neu-Laxova syndrome (Orphanet:2671)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Polysyndactyly - cardiac malformation (Orphanet:2934)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Saldino-Noonan type (Orphanet:93270)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 2 (OMIM:613853)
TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 3 (OMIM:613854)
Truncus arteriosus (Orphanet:3384)
VACTERL/VATER association (Orphanet:887)
Zunich-Kaye syndrome (Orphanet:3474)