Transposition of the great arteries
Symptom Information:
Symptom ID: | HPO:0001669 | |||||||||||||||||||
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) 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) |
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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) |