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Details
Link-It Detail - Human Phenotype - Abnormality of small intestinal villus morphology
Debug Stats
  • ### Total Build Time: 43 ms 15.100 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 224 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=6 ms Completed: 6 ms rowSize= 455 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 438 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=22 ms Completed: 22 ms rowSize= 2.105 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 10.716 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.043 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of small intestinal villus morphology HP:0011472
Parents (1)
img Abnormality of the small intestine HP:0002244
Children (1)
img Villous atrophy HP:0011473
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the small intestine HP:0002244
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the small intestine HP:0002244
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanFOXP350943forkhead box P3
img HP RolledUp, OMIM ID: 304790
HumanSPINK511005serine peptidase inhibitor, Kazal type 5
img HP RolledUp, OMIM ID: 256500
HumanALG310195ALG3, alpha-1,3- mannosyltransferase
img HP RolledUp, OMIM ID: 601110
HumanTTC379652tetratricopeptide repeat domain 37
img HP RolledUp, OMIM ID: 222470
HumanRFXANK8625regulatory factor X-associated ankyrin-containing protein
img HP RolledUp, OMIM ID: 209920
HumanADAM176868ADAM metallopeptidase domain 17
img HP RolledUp, OMIM ID: 614328
HumanSKIV2L6499superkiller viralicidic activity 2-like (S. cerevisiae)
img HP RolledUp, OMIM ID: 614602
HumanRFXAP5994regulatory factor X-associated protein
img HP RolledUp, OMIM ID: 209920
HumanRFX55993regulatory factor X, 5 (influences HLA class II expression)
img HP RolledUp, OMIM ID: 209920
HumanPCSK15122proprotein convertase subtilisin/kexin type 1
img HP RolledUp, OMIM ID: 600955
HumanMPI4351mannose phosphate isomerase
img HP RolledUp, OMIM ID: 602579
HumanCIITA4261class II, major histocompatibility complex, transactivator
img HP RolledUp, OMIM ID: 209920
HumanEPCAM4072epithelial cell adhesion molecule
img HP RolledUp, OMIM ID: 613217
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011472Abnormality of small intestinal villus morphology0self