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Details
Link-It Detail - Disease - Agammaglobulinemia
Debug Stats
  • ### Total Build Time: 296 ms 30.718 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 282 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=106 ms Completed: 106 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=17 ms Completed: 17 ms rowSize= 1.423 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=25 ms Completed: 25 ms rowSize= 5.399 KB
  • CONCEPT_RELATIONSHIPS gt=120 ms Completed: 120 ms rowSize= 12.982 KB
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 8.940 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Agammaglobulinemia C0001768
Definition (1)
An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Blood Protein Disorders C0005830
img Immunologic Deficiency Syndromes C0021051
img Lymphoproliferative Disorders C0024314
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Blood Protein Disorders C0005830
img Immune System Diseases C0021053img Immunologic Deficiency Syndromes C00210513img Immunologic Deficiency Syndromes C0021051
img Immune System Diseases C0021053img Immunoproliferative Disorders C00210704img Lymphoproliferative Disorders C0024314
img Hemic and Lymphatic Diseases C0018981img Lymphatic Diseases C00242284img Lymphoproliferative Disorders C0024314
Relationships (46)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 5
diso_​to_​diso : 31
diso_​to_​phen : 2
diso_​to_​phys : 3


Relationships:
none : 32
isa : 1
mapped_​to : 10
permuted_​term_​of : 1
replaces : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO99img Complication Aspects C1171258
DISO_to_PHEN98img genetic aspects C0017399
DISO_to_PHEN91img genetic aspects C0017399
DISO_to_DISO83img Complication Aspects C1171258
DISO_to_DISO63img Disease, X-Linked Genetic C1138434
DISO_to_DISO35img Disease, X-Linked Genetic C1138434
DISO_to_CHEM30img Protein Tyrosine Kinase C0033681
DISO_to_DISO29img Common Variable Immunodeficiency C0009447
DISO_to_DISO26img Thymoma C0040100
DISO_to_ANAT25img In Blood C0005768
DISO_to_DISO24img NEOPL THYMIC C0040116
DISO_to_ANAT23img B-Lymphocytes C0004561
DISO_to_ANAT22img In Blood C0005768
DISO_to_ANAT21img B-Lymphocytes C0004561
DISO_to_DISO18img Thymoma C0040100
DISO_to_DISO17img Immunologic Deficiency Syndromes C0021051
DISO_to_DISO17img Thymus Neoplasms C0040116
DISO_to_DISO16img DEFIC SYNDROME IMMUNOL C0021051
DISO_to_PHYS16img Mutation C0026882
DISO_to_ANAT15img Chromosome, Human X C1136735
DISO_to_CHEM15img Immunoglobulins, Intravenous C0085297
DISO_to_PHYS15img Mutation C0026882
DISO_to_DISO14img Common Variable Immunodeficiency C0009447
DISO_to_CHEM13img Immunoglobulins C0021027
DISO_to_CHEM13img Immunoglobulins, Intravenous C0085297
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
img GENERIF, Score=1000, Pubmed Id: 18606301, UMLKSK CUI: C0001768
HumanRFXANK8625regulatory factor X-associated ankyrin-containing protein
img OMIM, Score=1000, UMLKSK CUI: C0001768
HumanRFXAP5994regulatory factor X-associated protein
img OMIM, Score=1000, UMLKSK CUI: C0001768
HumanRFX55993regulatory factor X, 5 (influences HLA class II expression)
img OMIM, Score=1000, UMLKSK CUI: C0001768
HumanCIITA4261class II, major histocompatibility complex, transactivator
img OMIM, Score=1000, UMLKSK CUI: C0001768
HumanIL2RG3561interleukin 2 receptor, gamma
img OMIM, Score=1000, UMLKSK CUI: C0001768
HumanCD79B974CD79b molecule, immunoglobulin-associated beta
img GENERIF, Score=1000, Pubmed Id: 17709424, UMLKSK CUI: C0001768
HumanBTK695Bruton agammaglobulinemia tyrosine kinase
img GAD, Score=1000, Pubmed Id: 16159644, UMLKSK CUI: C0001768
img GENERIF, Score=1000, Pubmed Id: 15082835, UMLKSK CUI: C0001768
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0001768Agammaglobulinemia0self