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Details
Link-It Detail - Disease - Primary immune deficiency disorder
Debug Stats
  • ### Total Build Time: 37 ms 12.682 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=16 ms Completed: 16 ms rowSize= 5.405 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 5.681 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Primary immune deficiency disorder C0398686
Relationships (13)

Relation Types:
diso_​to_​diso : 13


Relationships:
isa : 13
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOisaimg C-53 DISORDERS OF COMPLEMENT C0272240
DISO_to_DISOisaimg Combined immunodeficiency disease C2711630
DISO_to_DISOisaimg Functional antibody defect C0398711
DISO_to_DISOisaimg Immunodeficiency associated with chromosomal abnormality C0398787
DISO_to_DISOisaimg Immunodeficiency with major anomalies C0398786
DISO_to_DISOisaimg Immunoglobulin Heavy Chain Deletion C0398692
DISO_to_DISOisaimg Immunoglobulin deficiency C0745242
DISO_to_DISOisaimg Immunoglobulin light chain deficiency C0398697
DISO_to_DISOisaimg Immunoglobulin-associated molecule deficiency C0398708
DISO_to_DISOisaimg Interleukin-12 deficiency C3266122
DISO_to_DISOisaimg Phagocytic cell defect C0398730
DISO_to_DISOisaimg Primary immunoglobulin catabolism abnormality C0398718
DISO_to_DISOisaimg TUFTSIN DEFICIENCY C0398741
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanNOX579400NADPH oxidase, EF-hand calcium binding domain 5
img GENERIF, Score=901, Pubmed Id: 17089090, UMLKSK CUI: C0398686
HumanIRAK451135interleukin-1 receptor-associated kinase 4
img GENERIF, Score=1000, Pubmed Id: 15825022, UMLKSK CUI: C0398686
img GENERIF, Score=734, Pubmed Id: 17917042, UMLKSK CUI: C0398686
HumanRAG25897recombination activating gene 2
img GENERIF, Score=901, Pubmed Id: 18463379, UMLKSK CUI: C0398686
HumanSP1103431SP110 nuclear body protein
img GENERIF, Score=901, Pubmed Id: 16648851, UMLKSK CUI: C0398686
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0398686Primary immune deficiency disorder0self