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Details
Link-It Detail - Disease - Genetic syndrome
Debug Stats
  • ### Total Build Time: 15 ms 7.504 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 330 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=0 Completed: 0 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=6 ms Completed: 6 ms rowSize= 4.299 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 1.662 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Genetic syndrome C0567439
Relationships (9)

Relation Types:
diso_​to_​diso : 9


Relationships:
associated_​with : 8
isa : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg DNA instability syndrome C1274227
DISO_to_DISOassociated_withimg Diabetes mellitus associated with genetic syndrome C0342274
DISO_to_DISOassociated_withimg Diabetes mellitus autosomal dominant type II (disorder) C0342277
DISO_to_DISOassociated_withimg Diabetes-deafness syndrome maternally transmitted (disorder) C0342289
DISO_to_DISOassociated_withimg Hyperproinsulinemia C0342283
DISO_to_DISOassociated_withimg Impaired glucose tolerance associated with genetic syndrome C0271657
DISO_to_DISOassociated_withimg MENDENHALL SYNDROME C0271695
DISO_to_DISOassociated_withimg Maturity onset diabetes mellitus in young C0342276
DISO_to_DISOassociated_withimg Wolfram Syndrome C0043207
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanTP638626tumor protein p63
img GENERIF, Score=877, Pubmed Id: 16679535, UMLKSK CUI: C0567439
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0567439Genetic syndrome0self