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Details
Link-It Detail - Human Phenotype - Abnormality of T cells
Debug Stats
  • ### Total Build Time: 38 ms 33.877 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 197 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 195 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=0 Completed: 0 ms rowSize= 447 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 5.081 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.019 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 23.797 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of T cells HP:0002843
Definition (1)
An abnormality of `T cells` (CL:0000084).
Parents (1)
img Abnormality of lymphocytes HP:0004332
Children (15)
img Increased number of peripheral CD3+ T cells HP:0002845
img Exaggerated cellular immune processes HP:0005397
img T lymphocytopenia HP:0005403
img Abnormality of T cell number HP:0011839
img Abnormality of CD4+ T cells HP:0005480
img Abnormal delayed hypersensitivity skin test HP:0002963
img Increased proportion of HLA DR+ and CD57+ T cells HP:0002853
img Absent cellular immunity HP:0005354
img Immune defect due to a T cell deficit HP:0005373
img Primary T-lymphocyte immune abnormalities HP:0005402
img Abnormality of T cell physiology HP:0011840
img Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors HP:0002851
img Impaired T cell function HP:0005435
img Abnormality of CD8+ T cells HP:0005481
img Increase in T cell number HP:0100828
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of lymphocytes HP:0004332
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of lymphocytes HP:0004332
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of lymphocytes HP:0004332
Genes (49)

Species:
human : 49
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCANDF1117084candidiasis, familial 1
img HP RolledUp, OMIM ID: 114580
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
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
img HP IEA, OMIM ID: 242900
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
img HP RolledUp, OMIM ID: 209920
HumanDGCR148220DiGeorge syndrome critical region gene 14
img HP RolledUp, OMIM ID: 192430
HumanDGCR68214DiGeorge syndrome critical region gene 6
img HP RolledUp, OMIM ID: 192430
HumanWIPF17456WAS/WASL interacting protein family, member 1
img HP RolledUp, OMIM ID: 614493
HumanWAS7454Wiskott-Aldrich syndrome
img HP RolledUp, OMIM ID: 301000
HumanUMPS7372uridine monophosphate synthetase
img HP IEA, OMIM ID: 258900
HumanTBX16899T-box 1
img HP RolledUp, OMIM ID: 192430
img HP RolledUp, OMIM ID: 188400
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
HumanRAG25897recombination activating gene 2
img HP RolledUp, OMIM ID: 233650
img HP RolledUp, OMIM ID: 601457
HumanRAG15896recombination activating gene 1
img HP RolledUp, OMIM ID: 601457
img HP RolledUp, OMIM ID: 233650
HumanRAB27A5873RAB27A, member RAS oncogene family
img HP RolledUp, OMIM ID: 607624
HumanPTPRC5788protein tyrosine phosphatase, receptor type, C
img HP RolledUp, OMIM ID: 608971
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002843Abnormality of T cells0self