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Details
Link-It Detail - Disease - Common Variable Immunodeficiency
Debug Stats
  • ### Total Build Time: 62 ms 38.791 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= 337 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 568 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.533 KB
  • CONCEPT_RELATIONSHIPS gt=32 ms Completed: 32 ms rowSize= 13.682 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 20.954 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Common Variable Immunodeficiency C0009447
Definition (1)
Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Immunologic Deficiency Syndromes C0021051
Ancestral Roots
RootRoot Plus OneDepthParent
img Immune System Diseases C0021053img Immunologic Deficiency Syndromes C00210513img Immunologic Deficiency Syndromes C0021051
Relationships (50)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 11
diso_​to_​diso : 21
diso_​to_​gene : 2
diso_​to_​phen : 2
diso_​to_​phys : 3


Relationships:
none : 39
classifies : 1
expanded_​form_​of : 1
gene_​associated_​with_​disease : 2
gene_​product_​malfunction_​associated_​with_​disease : 1
isa : 3
mapped_​to : 2
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO165img Complication Aspects C1171258
DISO_to_DISO138img Complication Aspects C1171258
DISO_to_PHEN106img genetic aspects C0017399
DISO_to_ANAT58img B-Lymphocytes C0004561
DISO_to_PHEN51img genetic aspects C0017399
DISO_to_CHEM39img Immunoglobulins, Intravenous C0085297
DISO_to_ANAT35img In Blood C0005768
DISO_to_DISO29img Agammaglobulinemia C0001768
DISO_to_CHEM23img Transmembrane Activator and CAML Interactor Protein C1706295
DISO_to_ANAT21img T-Lymphocyte C0039194
DISO_to_ANAT20img In Blood C0005768
DISO_to_DISO19img Granuloma C0018188
DISO_to_CHEM15img Immunoglobulins C0021027
DISO_to_DISO14img Agammaglobulinaemia C0001768
DISO_to_DISO14img Lung Diseases C0024115
DISO_to_CHEM13img Immunoglobulins, Intravenous C0085297
DISO_to_DISO13img Granuloma C0018188
DISO_to_ANAT12img B-Lymphocytes C0004561
DISO_to_CHEM12img Immunoglobulin G C0020852
DISO_to_DISO12img Sarcoidosis C0036202
DISO_to_DISO11img IgA Deficiency C0162538
DISO_to_ANAT10img T-Lymphocyte C0039194
DISO_to_CHEM10img Membrane Associated Proteins C0025252
DISO_to_ANAT9img CD4 Positive T Lymphocytes C0039215
DISO_to_CHEM9img Immunologic Factors C0021054
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img GAD, Score=1000, Pubmed Id: 16160919, UMLKSK CUI: C0009447
img GENERIF, Score=756, Pubmed Id: 16160919, UMLKSK CUI: C0009447
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img GENERIF, Score=1000, Pubmed Id: 18190602, UMLKSK CUI: C0009447
HumanICOS29851inducible T-cell co-stimulator
img GENERIF, Score=1000, Pubmed Id: 15507387, UMLKSK CUI: C0009447
HumanTNFRSF13B23495tumor necrosis factor receptor superfamily, member 13B
img GENERIF, Score=1000, Pubmed Id: 16007087, UMLKSK CUI: C0009447
img GENERIF, Score=1000, Pubmed Id: 16007086, UMLKSK CUI: C0009447
img GENERIF, Score=1000, Pubmed Id: 17983875, UMLKSK CUI: C0009447
img GENERIF, Score=1000, Pubmed Id: 17917015, UMLKSK CUI: C0009447
img GENERIF, Score=1000, Pubmed Id: 17392798, UMLKSK CUI: C0009447
HumanTNFSF13B10673tumor necrosis factor (ligand) superfamily, member 13b
img GENERIF, Score=694, Pubmed Id: 17556024, UMLKSK CUI: C0009447
HumanVAV17409vav 1 guanine nucleotide exchange factor
img GENERIF, Score=1000, Pubmed Id: 15817684, UMLKSK CUI: C0009447
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
img GENERIF, Score=1000, Pubmed Id: 17825894, UMLKSK CUI: C0009447
HumanCX3CL16376chemokine (C-X3-C motif) ligand 1
img GENERIF, Score=694, Pubmed Id: 18938112, UMLKSK CUI: C0009447
HumanPRKAR1A5573protein kinase, cAMP-dependent, regulatory, type I, alpha
img GENERIF, Score=756, Pubmed Id: 12759461, UMLKSK CUI: C0009447
HumanIL73574interleukin 7
img GENERIF, Score=1000, Pubmed Id: 15598813, UMLKSK CUI: C0009447
HumanCD70970CD70 molecule
img GENERIF, Score=1000, Pubmed Id: 12100033, UMLKSK CUI: C0009447
HumanCD40LG959CD40 ligand
img GENERIF, Score=756, Pubmed Id: 17893433, UMLKSK CUI: C0009447
HumanTNFRSF8943tumor necrosis factor receptor superfamily, member 8
img GENERIF, Score=756, Pubmed Id: 17912490, UMLKSK CUI: C0009447
HumanCD19930CD19 molecule
img GENERIF, Score=1000, Pubmed Id: 17882224, UMLKSK CUI: C0009447
HumanBTK695Bruton agammaglobulinemia tyrosine kinase
img GENERIF, Score=660, Pubmed Id: 18051214, UMLKSK CUI: C0009447
HumanXIAP331X-linked inhibitor of apoptosis
img GENERIF, Score=1000, Pubmed Id: 18520160, UMLKSK CUI: C0009447
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0009447Common Variable Immunodeficiency0self