Dextrocardia
Symptom Information:
Symptom ID: | HPO:0001651 | |||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Abnormal anatomic location of the heart(HPO:0004307) Dextrocardia(HPO:0001651) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Cardiac and vascular disorders congenital(MedDRA:10007510) Cardiac malpositions congenital(MedDRA:10019294) Dextrocardia(HPO:0001651) |
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Database Frequency: | 38 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2 | (OMIM:606217) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CATEL-MANZKE SYNDROME | (OMIM:616145) |
CHROMOSOME 15q25 DELETION SYNDROME | (OMIM:614294) |
CILIARY DYSKINESIA, PRIMARY, 1 | (OMIM:244400) |
CILIARY DYSKINESIA, PRIMARY, 13 | (OMIM:613193) |
CILIARY DYSKINESIA, PRIMARY, 17 | (OMIM:614679) |
CILIARY DYSKINESIA, PRIMARY, 2 | (OMIM:606763) |
CILIARY DYSKINESIA, PRIMARY, 20 | (OMIM:615067) |
CILIARY DYSKINESIA, PRIMARY, 25 | (OMIM:615482) |
Catel-Manzke syndrome | (Orphanet:1388) |
Congenital pseudoarthrosis of clavicle | (Orphanet:66630) |
DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA | (OMIM:221950) |
Diabetic embryopathy | (Orphanet:1926) |
Ellis Van Creveld syndrome | (Orphanet:289) |
HETEROTAXY, VISCERAL, 1, X-LINKED | (OMIM:306955) |
HETEROTAXY, VISCERAL, 4, AUTOSOMAL | (OMIM:613751) |
HETEROTAXY, VISCERAL, 5, AUTOSOMAL | (OMIM:270100) |
HETEROTAXY, VISCERAL, 6, AUTOSOMAL | (OMIM:614779) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
Ivemark syndrome | (Orphanet:97548) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Knobloch syndrome | (Orphanet:1571) |
Lethal restrictive dermopathy | (Orphanet:1662) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
Marden-Walker syndrome | (Orphanet:2461) |
Meacham syndrome | (Orphanet:3097) |
Meckel syndrome | (Orphanet:564) |
Mosaic trisomy 9 | (Orphanet:99776) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
PAGOD syndrome | (Orphanet:991) |
Poland syndrome | (Orphanet:2911) |
Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
Thoraco-abdominal enteric duplication | (Orphanet:1759) |