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Details
Link-It Detail - Disease - Hyperbilirubinemia
Debug Stats
  • ### Total Build Time: 284 ms 37.881 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 387 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.389 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.530 KB
  • CONCEPT_RELATIONSHIPS gt=211 ms Completed: 211 ms rowSize= 12.969 KB
  • CONCEPT_GENES gt=41 ms Completed: 41 ms rowSize= 19.383 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperbilirubinemia C0020433
Definition (1)
A condition characterized by an abnormal increase of BILIRUBIN in the blood, which may result in JAUNDICE. Bilirubin, a breakdown product of HEME, is normally excreted in the BILE or further catabolized before excretion in the urine.
Semantic Types (1)
Pathologic Function (T046)
Parents (1)
img Pathologic Processes C0030660
Children (3)
img Kernicterus C0022610
img Hyperbilirubinemia, Neonatal C0857007
img Jaundice C0022346
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306603img Pathologic Processes C0030660
Relationships (69)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 37
diso_​to_​diso : 26
diso_​to_​phen : 2


Relationships:
none : 29
isa : 7
mapped_​to : 5
may_​diagnose : 1
may_​treat : 26
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM62img Bilirubin C0005437
DISO_to_ANAT57img In Blood C0005768
DISO_to_DISO45img Complication Aspects C1171258
DISO_to_ANAT39img In Blood C0005768
DISO_to_CHEM38img Bilirubin C0005437
DISO_to_DISO31img Complication Aspects C1171258
DISO_to_DISO29img chemically induced C0007994
DISO_to_PHEN27img genetic aspects C0017399
DISO_to_DISO22img chemically induced C0007994
DISO_to_CHEM19img Glucuronosyltransferase C0041560
DISO_to_PHEN19img genetic aspects C0017399
DISO_to_ANAT12img Liver C0023884
DISO_to_CHEM12img Glucuronosyltransferase C0041560
DISO_to_DISO12img Gilbert Disease C0017551
DISO_to_ANAT11img Liver C0023884
DISO_to_CHEM11img Pyridines C0034255
DISO_to_CHEM10img Oligopeptides C0028954
DISO_to_CHEM8img ATP-Binding Cassette Transporters C0242738
DISO_to_DISO8img COMPL POSTOP C0032787
DISO_to_DISO8img Gilbert Disease C0017551
DISO_to_CHEM7img Antineoplastic Agents C0003392
DISO_to_CHEM7img Multidrug Resistance-Associated Proteins C0290741
DISO_to_DISO7img BILIRUBIN ENCEPH C0022610
DISO_to_DISO7img CNS disorder C0007682
DISO_to_DISO7img HIV Infections C0019693
Genes (49)

Species:
human : 49
Page Size
Current 25
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Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCDAN1146059codanin 1
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanHSD3B780270hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanIL2564806interleukin 25
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanC10orf256652chromosome 10 open reading frame 2
img OMIM, Score=1000, UMLKSK CUI: C0020433
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
Click here to display 18 evidence detail records.
HumanVPS33B26276vacuolar protein sorting 33 homolog B (yeast)
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanTREX111277three prime repair exonuclease 1
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanNPC210577Niemann-Pick disease, type C2
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanSLC25A1310165solute carrier family 25 (aspartate/glutamate carrier), member 13
img OMIM, Score=1000, UMLKSK CUI: C0020433
HumanCLDN19076claudin 1
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanSUCLA28803succinate-CoA ligase, ADP-forming, beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0020433
HumanABCB118647ATP-binding cassette, sub-family B (MDR/TAP), member 11
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanTK27084thymidine kinase 2, mitochondrial
img OMIM, Score=1000, UMLKSK CUI: C0020433
HumanSMPD16609sphingomyelin phosphodiesterase 1, acid lysosomal
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanSLCO2A16578solute carrier organic anion transporter family, member 2A1
img GAD, Score=1000, Pubmed Id: 15864125, UMLKSK CUI: C0020433
HumanSC5DL6309
img OMIM, Score=1000, UMLKSK CUI: C0020433
HumanRHAG6005Rh-associated glycoprotein
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanPRLR5618prolactin receptor
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanPLOD15351procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
img OMIM, Score=1000, UMLKSK CUI: C0020433
HumanPKLR5313pyruvate kinase, liver and RBC
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanABCB45244ATP-binding cassette, sub-family B (MDR/TAP), member 4
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanPFKM5213phosphofructokinase, muscle
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanATP8B15205ATPase, aminophospholipid transporter, class I, type 8B, member 1
INFERRED, Score=800, UMLKSK CUI: C0020433
HumanNPC14864Niemann-Pick disease, type C1
INFERRED, Score=800, UMLKSK CUI: C0020433
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020433Hyperbilirubinemia0self