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Details
Link-It Detail - Disease - Hyperbilirubinemia, Neonatal
Debug Stats
  • ### Total Build Time: 141 ms 24.596 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 511 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=66 ms Completed: 66 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 997 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 556 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.854 KB
  • CONCEPT_RELATIONSHIPS gt=29 ms Completed: 29 ms rowSize= 7.392 KB
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 10.616 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperbilirubinemia, Neonatal C0857007
Definition (1)
Accumulation of BILIRUBIN, a breakdown product of HEME PROTEINS, in the BLOOD during the first weeks of life. This may lead to NEONATAL JAUNDICE. The excess bilirubin may exist in the unconjugated (indirect) or the conjugated (direct) form. The condition may be self-limiting (PHYSIOLOGICAL NEONATAL JAUNDICE) or pathological with toxic levels of bilirubin.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Hyperbilirubinemia C0020433
img Infant, Newborn, Diseases C0021290
Children (1)
img Jaundice, Neonatal C0022353
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306604img Hyperbilirubinemia C0020433
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Infant, Newborn, Diseases C00212903img Infant, Newborn, Diseases C0021290
Relationships (16)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 3
diso_​to_​diso : 10
diso_​to_​phen : 1


Relationships:
none : 12
associated_​with : 1
isa : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT77img In Blood C0005768
DISO_to_CHEM77img Bilirubin C0005437
DISO_to_DISO37img Complication Aspects C1171258
DISO_to_PHEN37img genetic aspects C0017399
DISO_to_DISO30img BILIRUBIN ENCEPH C0022610
DISO_to_CHEM24img Glucuronosyltransferase C0041560
DISO_to_CHEM18img Bilirubin C0005437
DISO_to_DISO16img Jaundice, Neonatal C0022353
DISO_to_DISO14img Glucosephosphate Dehydrogenase Deficiency C0017758
DISO_to_DISO14img Infant, Premature, Diseases C0021295
DISO_to_ANAT13img In Blood C0005768
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_DISOassociated_withimg Bronze baby C0410946
DISO_to_DISOpermuted_term_ofimg During Infancies, Hyperbilirubinemia C0857007
DISO_to_DISOisaimg Jaundice, Neonatal C0022353
DISO_to_DISOisaimg Neonatal unconjugated hyperbilirubinaemia C0559506
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanCDAN1146059codanin 1
INFERRED, Score=800, UMLKSK CUI: C0857007
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
img GENERIF, Score=1000, Pubmed Id: 17888052, UMLKSK CUI: C0857007
img GENERIF, Score=1000, Pubmed Id: 18558634, UMLKSK CUI: C0857007
img GENERIF, Score=1000, Pubmed Id: 12105841, UMLKSK CUI: C0857007
img GENERIF, Score=1000, Pubmed Id: 15771689, UMLKSK CUI: C0857007
img GENERIF, Score=901, Pubmed Id: 18043502, UMLKSK CUI: C0857007
img GAD, Score=1000, Pubmed Id: 10353933, UMLKSK CUI: C0857007
img GENERIF, Score=1000, Pubmed Id: 17990575, UMLKSK CUI: C0857007
HumanNPC210577Niemann-Pick disease, type C2
INFERRED, Score=800, UMLKSK CUI: C0857007
HumanSMPD16609sphingomyelin phosphodiesterase 1, acid lysosomal
INFERRED, Score=800, UMLKSK CUI: C0857007
HumanNPC14864Niemann-Pick disease, type C1
INFERRED, Score=800, UMLKSK CUI: C0857007
HumanHMOX13162heme oxygenase (decycling) 1
img GENERIF, Score=1000, Pubmed Id: 12736395, UMLKSK CUI: C0857007
HumanGSTM12944glutathione S-transferase mu 1
INFERRED, Score=800, UMLKSK CUI: C0857007
HumanABCC21244ATP-binding cassette, sub-family C (CFTR/MRP), member 2
INFERRED, Score=800, UMLKSK CUI: C0857007
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0857007Hyperbilirubinemia, Neonatal0self