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Details
Link-It Detail - Disease - IgA Deficiency
Debug Stats
  • ### Total Build Time: 99 ms 22.990 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 227 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=14 ms Completed: 14 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=29 ms Completed: 29 ms rowSize= 2.803 KB
  • CONCEPT_RELATIONSHIPS gt=28 ms Completed: 28 ms rowSize= 9.788 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 7.949 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
IgA Deficiency C0162538
Definition (1)
A dysgammaglobulinemia characterized by a deficiency of IMMUNOGLOBULIN A.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Dysgammaglobulinemia C0013374
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Dysgammaglobulinemia C0013374
img Immune System Diseases C0021053img Immunologic Deficiency Syndromes C00210514img Dysgammaglobulinemia C0013374
Relationships (23)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 7
diso_​to_​diso : 11
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 20
mapped_​to : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO50img Complication Aspects C1171258
DISO_to_DISO31img Complication Aspects C1171258
DISO_to_PHEN29img genetic aspects C0017399
DISO_to_CHEM23img Immunoglobulin A C0020835
DISO_to_ANAT22img In Blood C0005768
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_DISO13img Celiac Disease C0007570
DISO_to_CHEM12img Immunoglobulin A C0020835
DISO_to_DISO12img Celiac Disease C0007570
DISO_to_DISO11img Common Variable Immunodeficiency C0009447
DISO_to_ANAT10img In Blood C0005768
DISO_to_DISO10img DEFIC IGG C0162539
DISO_to_CHEM7img Abs - Autoantibodies C0004358
DISO_to_CHEM6img Antibodies, Anti-Idiotypic C0003242
DISO_to_DISO6img Common Variable Immunodeficiency C0009447
DISO_to_CHEM5img Immunoglobulin G C0020852
DISO_to_CHEM5img Transglutaminases C0033679
DISO_to_CHEM5img Transmembrane Activator and CAML Interactor Protein C1706295
DISO_to_DISO5img Lupus Erythematosus, Systemic C0024141
DISO_to_PHYS5img GENET PREDISPOSITION C0314657
DISO_to_DISOmapped_toimg IGAD2 C1836032
DISO_to_DISOpermuted_term_ofimg IgA Deficiency C0162538
DISO_to_DISOmapped_toimg Immunoglobulin a deficiency 1 C2931161
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanTNFRSF13B23495tumor necrosis factor receptor superfamily, member 13B
img GENERIF, Score=1000, Pubmed Id: 17392798, UMLKSK CUI: C0162538
img GENERIF, Score=1000, Pubmed Id: 16007086, UMLKSK CUI: C0162538
HumanIL103586interleukin 10
img GENERIF, Score=1000, Pubmed Id: 16803619, UMLKSK CUI: C0162538
HumanIL63569interleukin 6 (interferon, beta 2)
img GENERIF, Score=1000, Pubmed Id: 18486766, UMLKSK CUI: C0162538
HumanHLA-DRB13123
img GENERIF, Score=1000, Pubmed Id: 18057683, UMLKSK CUI: C0162538
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0162538
HumanHLA-DQA13117
img OMIM, Score=1000, UMLKSK CUI: C0162538
HumanHLA-B3106
img GENERIF, Score=1000, Pubmed Id: 18057683, UMLKSK CUI: C0162538
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0162538IgA Deficiency0self