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Details
Link-It Detail - Disease - Eisenmenger Complex
Debug Stats
  • ### Total Build Time: 38 ms 18.309 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 386 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=0 Completed: 0 ms rowSize= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 4.124 KB
  • CONCEPT_RELATIONSHIPS gt=15 ms Completed: 15 ms rowSize= 8.656 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 2.719 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Eisenmenger Complex C0013743
Complex, Eisenmenger
Definition (1)
A condition associated with VENTRICULAR SEPTAL DEFECT and other congenital heart defects that allow the mixing of pulmonary and systemic circulation, increase blood flow into the lung, and subsequent responses to low oxygen in blood. This complex is characterized by progressive PULMONARY HYPERTENSION; HYPERTROPHY of the RIGHT VENTRICLE; CYANOSIS; and ERYTHROCYTOSIS.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Heart Defects, Congenital C0018798
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
Relationships (20)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 7
diso_​to_​diso : 9


Relationships:
none : 14
associated_​with : 3
location_​of : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO64img Complication Aspects C1171258
DISO_to_DISO29img Hypertension, Pulmonary C0020542
DISO_to_DISO28img Complication Aspects C1171258
DISO_to_ANAT16img Pulmonary Artery C0034052
DISO_to_CHEM16img Sulfonamides C0038760
DISO_to_CHEM14img Piperazines C0031958
DISO_to_CHEM14img Sulfones C0038761
DISO_to_CHEM10img Antihypertensive Agents C0003364
DISO_to_DISO10img Hypertension, Pulmonary C0020542
DISO_to_ANAT9img In Blood C0005768
DISO_to_CHEM9img 815-816 VASODILATING AGENTS C0042402
DISO_to_CHEM9img Antihypertensive Agents C0003364
DISO_to_CHEM9img Sulfonamides C0038760
DISO_to_DISO9img Heart Septal Defects, Ventricular C0018818
DISO_to_ANATlocation_ofimg Right ventricular structure C0225883
DISO_to_ANATlocation_ofimg Ventricular Septum C0225870
DISO_to_DISOassociated_withimg 207 CONGENITAL ABNORMAL COMMUNICATIONS C0332906
DISO_to_DISOpermuted_term_ofimg Complex, Eisenmenger C0013743
DISO_to_DISOassociated_withimg Congenital failure of fusion C0332915
DISO_to_DISOassociated_withimg Congenital hypertrophy C0332887
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanTGFBR37049transforming growth factor, beta receptor III
img GENERIF, Score=660, Pubmed Id: 18097622, UMLKSK CUI: C0013743
HumanBMPR2659bone morphogenetic protein receptor, type II (serine/threonine kinase)
img GENERIF, Score=840, Pubmed Id: 17102831, UMLKSK CUI: C0013743
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0013743Eisenmenger Complex0self