Dextrocardia

Symptom Information:

Symptom ID: HPO:0001651
Synonyms:
Thoracic situs inversus [HPO:0001651]
Dextrocardia (disorder) [Orphanet:34220]
Dextrocardia [Orphanet:34220]
Dextrocardia [OMIM:Dextrocardia]
Dextrocardia/abnormal heart position/cardiac heterotaxia/situs inversus [Orphanet:34220]
Dextrocardia [MedDRA:10012592]
Dextrocardia (in left-sided Poland sequence) [OMIM:Dextrocardia (in left-sided Poland sequence)]
Dextrocardia (in some patients) [OMIM:Dextrocardia (in some patients)]
Dextrocardia (in some) [OMIM:Dextrocardia (in some)]
Quality:
Cross references:
Orphanet:34220 "Dextrocardia/abnormal heart position/cardiac heterotaxia/situs inversus" [Orphanet:34220]
OMIM: "Dextrocardia" [OMIM:Dextrocardia]
OMIM: "Dextrocardia (in left-sided Poland sequence)" [OMIM:Dextrocardia (in left-sided Poland sequence)]
OMIM: "Dextrocardia (in some patients)" [OMIM:Dextrocardia (in some patients)]
OMIM: "Dextrocardia (in some)" [OMIM:Dextrocardia (in some)]
UMLS:C0011813 "Dextrocardia" [HPO:0001651]
UMLS:C0011813 "Dextrocardia" [Orphanet:34220]
Is a (Direct Parents):
MedDRA Cardiac malpositions congenital
Orphanet Structural anomalies of the cardio-circulatory system
HPO         Abnormal anatomic location of the heart
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)
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)