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Details
Link-It Detail - Disease - Abnormal hepatic function
Debug Stats
  • ### Total Build Time: 51 ms 14.487 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 348 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 203 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 2.209 KB
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 10.511 KB
  • CONCEPT_XREFS gt=10 ms Completed: 10 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Abnormal hepatic function C0086565
Definition (1)
A finding that indicates abnormal liver function.
Relationships (3)

Relation Types:
diso_​to_​diso : 3


Relationships:
isa : 1
parent_​is_​cdrh : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg Abnormal bile secretion C0232756
DISO_to_DISOpermuted_term_ofimg Abnormal hepatic function C0086565
DISO_to_DISOparent_is_cdrhimg Patient Problem C1254481
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanADIPOR279602adiponectin receptor 2
img GENERIF, Score=1000, Pubmed Id: 18719649, UMLKSK CUI: C0086565
HumanHAMP57817hepcidin antimicrobial peptide
img GENERIF, Score=1000, Pubmed Id: 15797999, UMLKSK CUI: C0086565
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img GENERIF, Score=1000, Pubmed Id: 12111344, UMLKSK CUI: C0086565
HumanIL63569interleukin 6 (interferon, beta 2)
img GENERIF, Score=694, Pubmed Id: 17442294, UMLKSK CUI: C0086565
HumanHSD17B43295hydroxysteroid (17-beta) dehydrogenase 4
img OMIM, Score=1000, UMLKSK CUI: C0086565
HumanCP1356ceruloplasmin (ferroxidase)
img GENERIF, Score=901, Pubmed Id: 17688883, UMLKSK CUI: C0086565
HumanCOX6B11340cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
img OMIM, Score=1000, UMLKSK CUI: C0086565
HumanMS4A1931membrane-spanning 4-domains, subfamily A, member 1
img GENERIF, Score=1000, Pubmed Id: 17712791, UMLKSK CUI: C0086565
HumanALDH2217aldehyde dehydrogenase 2 family (mitochondrial)
img GENERIF, Score=1000, Pubmed Id: 12198368, UMLKSK CUI: C0086565
HumanACAA130acetyl-CoA acyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0086565
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0086565Abnormal hepatic function0self