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Details
Link-It Detail - Disease - Dextrocardia
Debug Stats
  • ### Total Build Time: 186 ms 26.329 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 522 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 993 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 557 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 5.438 KB
  • CONCEPT_RELATIONSHIPS gt=117 ms Completed: 117 ms rowSize= 9.505 KB
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 7.688 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Dextrocardia C0011813
Definition (1)
A congenital defect in which the heart is located on the right side of the THORAX instead of on the left side (levocardia, the normal position). When dextrocardia is accompanied with inverted HEART ATRIA, a right-sided STOMACH, and a left-sided LIVER, the combination is called dextrocardia with SITUS INVERSUS. Dextrocardia may adversely affect other thoracic organs.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (2)
img Heart Defects, Congenital C0018798
img Situs Inversus C0037221
Children (1)
img Kartagener Syndrome C0022521
Ancestral Roots
RootRoot Plus OneDepthParent
img Cardiovascular Diseases C0007222img Heart Diseases C00187994img Heart Defects, Congenital C0018798
img Cardiovascular Diseases C0007222img Cardiovascular Abnormalities C02430504img Heart Defects, Congenital C0018798
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Heart Defects, Congenital C0018798
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Situs Inversus C0037221
Relationships (22)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 20


Relationships:
none : 12
associated_​with : 1
isa : 3
location_​of : 2
mapped_​to : 3
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO62img Complication Aspects C1171258
DISO_to_DISO39img Complication Aspects C1171258
DISO_to_DISO32img Situs Inversus C0037221
DISO_to_DISO25img Abnormalities, Multiple C0000772
DISO_to_DISO18img Situs Inversus C0037221
DISO_to_DISO10img Abnormalities, Multiple C0000772
DISO_to_DISO10img Atrial Fibrillation C0004238
DISO_to_DISO10img Transposition of Great Vessels C0040761
DISO_to_DISO7img Congenital Heart Defects C0018798
DISO_to_DISO7img Coronary Disease C0010068
DISO_to_DISO7img Heart Septal Defects, Atrial C0018817
DISO_to_DISO7img Poland Syndrome C0032357
DISO_to_ANATlocation_ofimg Heart C0018787
DISO_to_ANATlocation_ofimg Structure of right thoracic cavity C0230140
DISO_to_DISOmapped_toimg AGONADISM WITH MULTIPLE INTERNAL MALFORMATIONS C1859967
DISO_to_DISOmapped_toimg Aughton syndrome C1857298
DISO_to_DISOassociated_withimg Congenital Transposition C0040759
DISO_to_DISOpermuted_term_ofimg DEXTROCARDIA C0011813
DISO_to_DISOisaimg Dextrocardia, isolated C0265863
DISO_to_DISOmapped_toimg HETEROTAXY, VISCERAL, 1, X-LINKED C1844020
DISO_to_DISOisaimg Kartagener Syndrome C0022521
DISO_to_DISOisaimg Mirror-imaged heart C0344609
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanDNAL183544dynein, axonemal, light chain 1
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanCRELD178987cysteine-rich with EGF-like domains 1
img OMIM, Score=1000, UMLKSK CUI: C0011813
HumanDNAI264446dynein, axonemal, intermediate chain 2
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanDNAH756171dynein, axonemal, heavy chain 7
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanTXNDC351314
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanDNAI127019dynein, axonemal, intermediate chain 1
img OMIM, Score=1000, UMLKSK CUI: C0011813
HumanDPCD25911deleted in primary ciliary dyskinesia homolog (mouse)
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanDNAH118701dynein, axonemal, heavy chain 11
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanZIC37547Zic family member 3
img OMIM, Score=1000, UMLKSK CUI: C0011813
HumanDNAH51767dynein, axonemal, heavy chain 5
INFERRED, Score=800, UMLKSK CUI: C0011813
HumanCFTR1080cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
INFERRED, Score=800, UMLKSK CUI: C0011813
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011813Dextrocardia0self