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Details
Link-It Detail - Human Phenotype - Abnormality of T cell physiology
Debug Stats
  • ### Total Build Time: 15 ms 26.604 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 2.086 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.007 KB
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  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 19.496 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of T cell physiology HP:0011840
Definition (1)
A deviation from the normal count of `T cells` (CL:0000084).
Parents (1)
img Abnormality of T cells HP:0002843
Children (6)
img Exaggerated cellular immune processes HP:0005397
img Abnormal delayed hypersensitivity skin test HP:0002963
img Absent cellular immunity HP:0005354
img Primary T-lymphocyte immune abnormalities HP:0005402
img Impaired T cell function HP:0005435
img Decreased T cell activation HP:0005419
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 (35)

Species:
human : 35
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCANDF1117084candidiasis, familial 1
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img HP RolledUp, OMIM ID: 240500
HumanMAGT184061magnesium transporter 1
img HP RolledUp, OMIM ID: 300853
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 181000
HumanEPG557724ectopic P-granules autophagy protein 5 homolog (C. elegans)
img HP RolledUp, OMIM ID: 242840
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img HP RolledUp, OMIM ID: 181000
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
img HP RolledUp, OMIM ID: 201100
HumanDGCR854487DGCR8 microprocessor complex subunit
img HP RolledUp, OMIM ID: 192430
HumanICOS29851inducible T-cell co-stimulator
img HP RolledUp, OMIM ID: 607594
img HP RolledUp, OMIM ID: 240500
HumanTNFRSF13B23495tumor necrosis factor receptor superfamily, member 13B
img HP RolledUp, OMIM ID: 240500
HumanDGCR29993DiGeorge syndrome critical region gene 2
img HP RolledUp, OMIM ID: 192430
HumanRFXANK8625regulatory factor X-associated ankyrin-containing protein
HumanDGCR148220DiGeorge syndrome critical region gene 14
img HP RolledUp, OMIM ID: 192430
HumanDGCR68214DiGeorge syndrome critical region gene 6
img HP RolledUp, OMIM ID: 192430
HumanWAS7454Wiskott-Aldrich syndrome
img HP RolledUp, OMIM ID: 301000
HumanUMPS7372uridine monophosphate synthetase
img HP RolledUp, OMIM ID: 258900
HumanTBX16899T-box 1
img HP RolledUp, OMIM ID: 192430
img HP RolledUp, OMIM ID: 188400
HumanRFXAP5994regulatory factor X-associated protein
HumanRFX55993regulatory factor X, 5 (influences HLA class II expression)
HumanRAB27A5873RAB27A, member RAS oncogene family
HumanPNP4860purine nucleoside phosphorylase
HumanCIITA4261class II, major histocompatibility complex, transactivator
HumanJAK33718Janus kinase 3
HumanIL7R3575interleukin 7 receptor
HumanHLA-DRB13123
img HP RolledUp, OMIM ID: 181000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011840Abnormality of T cell physiology0self