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Details
Link-It Detail - Disease - Autoimmune Diseases
Debug Stats
  • ### Total Build Time: 504 ms 49.977 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 318 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=16 ms Completed: 16 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=51 ms Completed: 51 ms rowSize= 9.705 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.113 KB
  • CONCEPT_RELATIONSHIPS gt=287 ms Completed: 287 ms rowSize= 15.740 KB
  • CONCEPT_GENES gt=140 ms Completed: 140 ms rowSize= 20.827 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Autoimmune Diseases C0004364
AUTOIMMUNE DIS
Definition (1)
Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Immune System Diseases C0021053
Children (22)
img Purpura, Thrombocytopenic, Idiopathic C0043117
img Addison Disease C0001403
img Autoimmune Diseases of the Nervous System C0751871
img Thyroiditis, Autoimmune C0920350
img Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis C2717865
img Glomerulonephritis, Membranous C0017665
img Ophthalmia, Sympathetic C0029077
img Lambert-Eaton Myasthenic Syndrome C0022972
img Lupus Erythematosus, Systemic C0024141
img Pemphigoid, Bullous C0030805
img Dermatitis Herpetiformis C0011608
img Arthritis, Rheumatoid C0003873
img Glomerulonephritis, IGA C0017661
img Anemia, Hemolytic, Autoimmune C0002880
img Polyendocrinopathies, Autoimmune C0085409
img Anti-Glomerular Basement Membrane Disease C0403529
img Antiphospholipid Syndrome C0085278
img Diabetes Mellitus, Type 1 C0011854
img Pemphigus C0030807
img Graves Disease C0018213
img Hepatitis, Autoimmune C0241910
img Autoimmune Lymphoproliferative Syndrome C1328840
Ancestral Roots
RootRoot Plus OneDepthParent
img Immune System Diseases C00210532img Immune System Diseases C0021053
Relationships (336)

Relation Types:
diso_​to_​anat : 32
diso_​to_​chem : 106
diso_​to_​diso : 172
diso_​to_​gene : 5
diso_​to_​phen : 2
diso_​to_​phys : 19


Relationships:
none : 244
associated_​with : 2
disease_​has_​associated_​disease : 6
entry_​version_​of : 1
gene_​associated_​with_​disease : 4
gene_​product_​malfunction_​associated_​with_​disease : 2
has_​cdrh_​parent : 1
isa : 28
mapped_​to : 5
may_​treat : 30
parent_​is_​cdrh : 1
related_​to : 7
use : 5
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN823img genetic aspects C0017399
DISO_to_DISO684img Complication Aspects C1171258
DISO_to_PHEN606img genetic aspects C0017399
DISO_to_DISO551img Complication Aspects C1171258
DISO_to_DISO424img Pancreatitis C0030305
DISO_to_CHEM379img Abs - Autoantibodies C0004358
DISO_to_CHEM342img Abs - Autoantibodies C0004358
DISO_to_ANAT309img In Blood C0005768
DISO_to_DISO282img Autoimmune Status C0004368
DISO_to_ANAT229img In Blood C0005768
DISO_to_CHEM217img Immunoglobulin G C0020852
DISO_to_DISO212img Inflammation C0021368
DISO_to_DISO186img Pancreatitis C0030305
DISO_to_DISO182img chemically induced C0007994
DISO_to_ANAT174img Regulatory T-Lymphocytes C0039198
DISO_to_CHEM162img Immunosuppressive Agents C0021081
DISO_to_DISO153img Autoimmune Status C0004368
DISO_to_ANAT148img T-Lymphocyte C0039194
DISO_to_DISO148img Uveitis C0042164
DISO_to_CHEM144img Antibodies, Monoclonal C0003250
DISO_to_DISO142img chemically induced C0007994
DISO_to_CHEM136img Immunosuppressive Agents C0021081
DISO_to_CHEM134img Antigens, Autologous C0004359
DISO_to_CHEM131img Antigens, Autologous C0004359
DISO_to_ANAT127img B-Lymphocytes C0004561
Genes (765)

Species:
human : 765
Page Size
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
img GENERIF, Score=1000, Pubmed Id: 12392510, UMLKSK CUI: C0004364
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanKIR2DS2100132285killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanNCF1653361neutrophil cytosolic factor 1
img GENERIF, Score=694, Pubmed Id: 19077231, UMLKSK CUI: C0004364
HumanNOS2P1645740nitric oxide synthase 2 pseudogene 1
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanMIR16-1406950
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanMIR146A406938microRNA 146a
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanSUMO4387082small ubiquitin-like modifier 4
img GENERIF, Score=673, Pubmed Id: 16735488, UMLKSK CUI: C0004364
HumanNCR3259197natural cytotoxicity triggering receptor 3
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanMYAS1246750Myasthenia gravis with thymus hyperplasia
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanC10orf27219793
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanAQPEP206338laeverin
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanNOS2P2201288nitric oxide synthase 2 pseudogene 2
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanCLEC4C170482C-type lectin domain family 4, member C
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanSLC30A8169026solute carrier family 30 (zinc transporter), member 8
img GENERIF, Score=901, Pubmed Id: 17942684, UMLKSK CUI: C0004364
HumanOLIG3167826oligodendrocyte transcription factor 3
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanIL23R149233interleukin 23 receptor
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanDSG4147409desmoglein 4
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanADAMTS14140766ADAM metallopeptidase with thrombospondin type 1 motif, 14
INFERRED, Score=800, UMLKSK CUI: C0004364
HumanSCGB3A2117156secretoglobin, family 3A, member 2
INFERRED, Score=800, UMLKSK CUI: C0004364
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0004364Autoimmune Diseases0self