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Details
Link-It Detail - Disease - Cyanosis
Debug Stats
  • ### Total Build Time: 198 ms 22.152 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 314 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 292 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.526 KB
  • CONCEPT_RELATIONSHIPS gt=162 ms Completed: 162 ms rowSize= 13.531 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 4.604 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.143 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cyanosis C0010520
Definition (1)
A bluish or purplish discoloration of the skin and mucous membranes resulting from a reduced amount of oxygenated hemoglobin in the blood.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Signs and Symptoms C0037088
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370883img Signs and Symptoms C0037088
Relationships (81)

Relation Types:
diso_​to_​anat : 8
diso_​to_​chem : 31
diso_​to_​diso : 40
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 35
classifies : 2
isa : 4
mapped_​to : 12
may_​prevent : 1
may_​treat : 26
parent_​is_​cdrh : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO69img Congenital Heart Defects C0018798
DISO_to_DISO27img Complication Aspects C1171258
DISO_to_DISO27img Congenital Heart Defects C0018798
DISO_to_ANAT23img In Blood C0005768
DISO_to_DISO18img Methemoglobinemia C0025637
DISO_to_DISO15img Methemoglobinemia C0025637
DISO_to_DISO15img chemically induced C0007994
DISO_to_ANAT12img Pulmonary Artery C0034052
DISO_to_DISO12img Apnea C0003578
DISO_to_DISO12img chemically induced C0007994
DISO_to_DISO11img Tetralogy of Fallot C0039685
DISO_to_DISO10img Anoxia C0003130
DISO_to_DISO8img Complication Aspects C1171258
DISO_to_DISO8img Dyspnea C0013404
DISO_to_DISO8img Heart Diseases C0018799
DISO_to_DISO7img Atrial Septal Defects C0018817
DISO_to_DISO6img Apnea C0003578
DISO_to_DISO6img Muscle Hypotonia C0026827
DISO_to_PHYS6img Pulmonary Circulation C0034057
DISO_to_ANAT5img Fingers C0016129
DISO_to_ANAT5img In Blood C0005768
DISO_to_ANAT5img Pulmonary Artery C0034052
DISO_to_DISO5img Hypertension, Pulmonary C0020542
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_ANAT4img Inferior vena cava structure C0042458
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanAVSD17446atrioventricular septal defect 1
img OMIM, Score=1000, UMLKSK CUI: C0010520
HumanSCN2A6326sodium channel, voltage-gated, type II, alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0010520
HumanGJA12697gap junction protein, alpha 1, 43kDa
img OMIM, Score=1000, UMLKSK CUI: C0010520
HumanENG2022endoglin
img OMIM, Score=1000, UMLKSK CUI: C0010520
HumanACVRL194activin A receptor type II-like 1
img OMIM, Score=1000, UMLKSK CUI: C0010520
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0010520Cyanosis0self