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Details
Link-It Detail - Jax Mouse Phenotype - increased hamartoma incidence
Debug Stats
  • ### Total Build Time: 13 ms 10.292 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 445 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=1 ms Completed: 1 ms rowSize= 591 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.326 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.571 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 3.694 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
increased hamartoma incidence MP:0010306
Definition (1)
greater than the expected number of benign focal malformations in a specific population in a given time period; results from faulty development of an organ, and is composed of an abnormal mixture of tissue elements, or an abnormal proportion of a single element normally present at that site
Parents (1)
img increased classified tumor incidence MP:0010273
Children (5)
img Lisch nodule MP:0006232
img retinal hamartoma MP:0006183
img colonic hamartoma MP:0002043
img skin hamartoma MP:0009469
img renal hamartoma MP:0003602
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img tumorigenesis MP:00020067img increased classified tumor incidence MP:0010273
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanTP537157tumor protein p53
Click here to display 16 evidence detail records.
HumanSTK116794serine/threonine kinase 11
Click here to display 16 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 16 evidence detail records.
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
INFERRED
HumanFOXO12308forkhead box O1
Click here to display 16 evidence detail records.
HumanCDX21045caudal type homeobox 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010306increased hamartoma incidence0self