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Details
Link-It Detail - Disease - Hyperphenylalaninaemia, type III
Debug Stats
  • ### Total Build Time: 45 ms 4.706 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=24 ms Completed: 24 ms rowSize= 1.703 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 1.413 KB
  • CONCEPT_XREFS gt=11 ms Completed: 11 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperphenylalaninaemia, type III C0268464
Relationships (2)

Relation Types:
diso_​to_​chem : 1
diso_​to_​diso : 1


Relationships:
associated_​with : 2
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEMassociated_withimg Phenylalanine Hydroxylase C0031456
DISO_to_DISOassociated_withimg 270 CONGENITAL DEFICIENCIES C0333006
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanPCBD15092pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha
img OMIM, Score=1000, UMLKSK CUI: C0268464
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268464Hyperphenylalaninaemia, type III0self