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Details
Link-It Detail - Human Phenotype - Abnormality of CD8+ T cells
Debug Stats
  • ### Total Build Time: 67 ms 10.876 KB
  • CONCEPT_NAME gt=2 ms Completed: 1 ms rowSize= 202 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
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=36 ms Completed: 36 ms rowSize= 781 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=16 ms Completed: 16 ms rowSize= 3.007 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 5.146 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of CD8+ T cells HP:0005481
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of T cells HP:0002843
Children (2)
img Absence of CD8+ T cells HP:0005422
img Decreased number of CD8+ T cells HP:0005415
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of T cells HP:0002843
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of T cells HP:0002843
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of T cells HP:0002843
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanWIPF17456WAS/WASL interacting protein family, member 1
img HP RolledUp, OMIM ID: 614493
HumanRAG25897recombination activating gene 2
img HP RolledUp, OMIM ID: 233650
HumanRAG15896recombination activating gene 1
img HP RolledUp, OMIM ID: 233650
HumanIL2RG3561interleukin 2 receptor, gamma
img HP RolledUp, OMIM ID: 312863
HumanCD8A925CD8a molecule
img HP RolledUp, OMIM ID: 608957
HumanATM472ataxia telangiectasia mutated
img HP RolledUp, OMIM ID: 208900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005481Abnormality of CD8+ T cells0self