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Details
Link-It Detail - Human Phenotype - Abnormal delayed hypersensitivity skin test
Debug Stats
  • ### Total Build Time: 23 ms 21.135 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 218 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 265 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=2 ms Completed: 2 ms rowSize= 778 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.435 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 5.809 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 11.479 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.037 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal delayed hypersensitivity skin test HP:0002963
Definition (1)
This is an immune function test measuring the presence of activated T cells that recognize a certain substance.
Parents (2)
img Abnormality of T cell physiology HP:0011840
img Abnormality of T cells HP:0002843
Children (4)
img Reduced delayed hypersensitivity HP:0002972
img Decreased reactivity to skin test antigens HP:0005434
img Cutaneous anergy HP:0002965
img Lack of delayed skin hypersensitivity reaction HP:0005427
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of T cell physiology HP:0011840
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of T cell physiology HP:0011840
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of T cell physiology HP:0011840
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 (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanCANDF1117084candidiasis, familial 1
img HP RolledUp, OMIM ID: 114580
HumanEPG557724ectopic P-granules autophagy protein 5 homolog (C. elegans)
img HP RolledUp, OMIM ID: 242840
HumanRFXANK8625regulatory factor X-associated ankyrin-containing protein
img HP RolledUp, OMIM ID: 209920
HumanWAS7454Wiskott-Aldrich syndrome
img HP IEA, OMIM ID: 301000
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
HumanRAB27A5873RAB27A, member RAS oncogene family
img HP RolledUp, OMIM ID: 607624
HumanCIITA4261class II, major histocompatibility complex, transactivator
img HP RolledUp, OMIM ID: 209920
HumanJAK33718Janus kinase 3
img HP RolledUp, OMIM ID: 600802
HumanIL7R3575interleukin 7 receptor
img HP RolledUp, OMIM ID: 600802
HumanCD3D915CD3d molecule, delta (CD3-TCR complex)
img HP RolledUp, OMIM ID: 600802
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
img HP RolledUp, OMIM ID: 603909
HumanFASLG356Fas ligand (TNF superfamily, member 6)
img HP RolledUp, OMIM ID: 601859
HumanFAS355Fas cell surface death receptor
img HP RolledUp, OMIM ID: 601859
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002963Abnormal delayed hypersensitivity skin test0self