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Details
Link-It Detail - Disease - Immunologic Deficiency Syndromes
Debug Stats
  • ### Total Build Time: 477 ms 43.087 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 243 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 558 bytes
  • CONCEPT_CHILDREN gt=17 ms Completed: 17 ms rowSize= 4.877 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.113 KB
  • CONCEPT_RELATIONSHIPS gt=352 ms Completed: 352 ms rowSize= 15.206 KB
  • CONCEPT_GENES gt=86 ms Completed: 86 ms rowSize= 19.378 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Immunologic Deficiency Syndromes C0021051
Definition (1)
A deficiency of immune response or a disorder characterized by deficient immune response.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Immune System Diseases C0021053
Children (11)
img HIV Infections C0019693
img Dysgammaglobulinemia C0013374
img Deltaretrovirus Infections C0020091
img Wiskott-Aldrich Syndrome C0043194
img Ataxia Telangiectasia C0004135
img Agammaglobulinemia C0001768
img Common Variable Immunodeficiency C0009447
img Severe Combined Immunodeficiency C0085110
img Lymphopenia C0024312
img Leukocyte-Adhesion Deficiency Syndrome C0242597
img Phagocyte Bactericidal Dysfunction C0031306
Ancestral Roots
RootRoot Plus OneDepthParent
img Immune System Diseases C00210532img Immune System Diseases C0021053
Relationships (238)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 33
diso_​to_​diso : 181
diso_​to_​gene : 2
diso_​to_​phen : 2
diso_​to_​phys : 9


Relationships:
none : 74
associated_​with : 1
classifies : 1
disease_​excludes_​finding : 2
disease_​has_​finding : 96
gene_​associated_​with_​disease : 2
isa : 18
mapped_​to : 24
may_​diagnose : 3
may_​treat : 14
parent_​is_​cdrh : 1
used_​for : 2
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN307img genetic aspects C0017399
DISO_to_PHEN222img genetic aspects C0017399
DISO_to_DISO200img Complication Aspects C1171258
DISO_to_DISO145img Complication Aspects C1171258
DISO_to_CHEM45img Immunoglobulins, Intravenous C0085297
DISO_to_ANAT42img In Blood C0005768
DISO_to_CHEM36img Immunoglobulins, Intravenous C0085297
DISO_to_PHYS31img Mutation C0026882
DISO_to_ANAT30img T-Lymphocyte C0039194
DISO_to_PHYS30img Mutation C0026882
DISO_to_CHEM29img Immunoglobulins C0021027
DISO_to_DISO29img AUTOIMMUNE DIS C0004364
DISO_to_ANAT27img T-Lymphocyte C0039194
DISO_to_DISO26img Infection, Opportunistic C0029118
DISO_to_CHEM25img Immunoglobulin G C0020852
DISO_to_CHEM24img Immunoglobulin M C0020861
DISO_to_ANAT21img B-Lymphocytes C0004561
DISO_to_DISO21img Infection C0021311
DISO_to_ANAT19img B-Lymphocytes C0004561
DISO_to_DISO19img Disease, X-Linked Genetic C1138434
DISO_to_CHEM18img Immunologic Factors C0021054
DISO_to_DISO18img Ectodermal Dysplasia C0013575
DISO_to_DISO17img Agammaglobulinaemia C0001768
DISO_to_DISO17img Infection, Opportunistic C0029118
DISO_to_PHYS17img Immunity, Innate C0020969
Genes (353)

Species:
human : 353
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanNCF1653361neutrophil cytosolic factor 1
Click here to display 6 evidence detail records.
HumanPSORS9359825psoriasis susceptibility 9
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanSDK1221935sidekick cell adhesion molecule 1
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanAPOBEC3F200316apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3F
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanAPOBEC3H164668apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3H
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanIL23R149233interleukin 23 receptor
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img GENERIF, Score=861, Pubmed Id: 16160919, UMLKSK CUI: C0021051
HumanFRMD790167FERM domain containing 7
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanTRIM585363tripartite motif containing 5
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanRNF3980352ring finger protein 39
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanNHEJ179840nonhomologous end-joining factor 1
img GENERIF, Score=827, Pubmed Id: 16439204, UMLKSK CUI: C0021051
HumanPSORS765245psoriasis susceptibility 7
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanDCLRE1C64421DNA cross-link repair 1C
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanSLC28A364078solute carrier family 28 (concentrative nucleoside transporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanPSORS563870psoriasis susceptibility 5
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanPSORS663869psoriasis susceptibility 6
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanAPOBEC3G60489apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanBACH260468BTB and CNC homology 1, basic leucine zipper transcription factor 2
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanWFDC158189WAP four-disulfide core domain 1
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanSH3RF157630SH3 domain containing ring finger 1
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanAICDA57379activation-induced cytidine deaminase
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanRETN56729resistin
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanNLRP255655NLR family, pyrin domain containing 2
INFERRED, Score=800, UMLKSK CUI: C0021051
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED, Score=800, UMLKSK CUI: C0021051
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0021051Immunologic Deficiency Syndromes0self