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Details
Link-It Detail - Disease - Autoimmune Diseases of the Nervous System
Debug Stats
  • ### Total Build Time: 51 ms 41.306 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 439 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 494 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=0 Completed: 0 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= 996 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 4.068 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.786 KB
  • CONCEPT_RELATIONSHIPS gt=17 ms Completed: 17 ms rowSize= 12.757 KB
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 18.425 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Autoimmune Diseases of the Nervous System C0751871
AUTOIMMUNE DIS NERVOUS SYSTEM
Definition (1)
Disorders caused by cellular or humoral immune responses primarily directed towards nervous system autoantigens. The immune response may be directed towards specific tissue components (e.g., myelin) and may be limited to the central nervous system (e.g., MULTIPLE SCLEROSIS) or the peripheral nervous system (e.g., GUILLAIN-BARRE SYNDROME).
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Autoimmune Diseases C0004364
img Nervous System Diseases C0027765
Children (9)
img Vasculitis, Central Nervous System C0751878
img Polyradiculoneuropathy C0032587
img Uveomeningoencephalitic Syndrome C0042170
img Nervous System Autoimmune Disease, Experimental C0752090
img Leukoencephalitis, Acute Hemorrhagic C0014077
img Myasthenia Gravis C0026896
img Lambert-Eaton Myasthenic Syndrome C0022972
img Demyelinating Autoimmune Diseases, CNS C0751873
img Stiff-Person Syndrome C0085292
Ancestral Roots
RootRoot Plus OneDepthParent
img Immune System Diseases C0021053img Autoimmune Diseases C00043643img Autoimmune Diseases C0004364
img Nervous System Diseases C0027765img Autoimmune Diseases C00043642img Nervous System Diseases C0027765
Relationships (38)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 8
diso_​to_​diso : 23
diso_​to_​phen : 1


Relationships:
none : 29
entry_​version_​of : 1
is_​associated_​anatomic_​site_​of : 1
isa : 3
mapped_​to : 4
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM49img Abs - Autoantibodies C0004358
DISO_to_DISO38img Complication Aspects C1171258
DISO_to_CHEM30img Abs - Autoantibodies C0004358
DISO_to_DISO30img Encephalitis C0014038
DISO_to_DISO26img Streptococcal Infections C0038395
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_PHEN25img genetic aspects C0017399
DISO_to_CHEM21img Immunoglobulins, Intravenous C0085297
DISO_to_ANAT16img Autonomic ganglion C0017068
DISO_to_CHEM16img N-Methyl-D-Aspartate Receptors C0080093
DISO_to_ANAT15img In Blood C0005768
DISO_to_DISO14img Obsessive-Compulsive Disorder C0028768
DISO_to_DISO13img Streptococcal Infections C0038395
DISO_to_CHEM12img Immunoglobulins, Intravenous C0085297
DISO_to_DISO12img Hearing Loss, Sensorineural C0018784
DISO_to_ANAT11img In Blood C0005768
DISO_to_DISO11img Congenital neurologic anomalies C0497552
DISO_to_DISO11img ENCEPH LIMBIC C0338430
DISO_to_ANAT10img T-Lymphocyte C0039194
DISO_to_CHEM9img Antigens, Autologous C0004359
DISO_to_CHEM9img Immunologic Factors C0021054
DISO_to_DISO9img Autonomic Nervous System Diseases C1145628
DISO_to_DISO9img Paraneoplastic Syndromes, Nervous System C0751911
DISO_to_DISO9img Tic Disorders C0040188
DISO_to_ANAT8img Brain C0006104
Genes (269)

Species:
human : 269
Page Size
Current 25
  Page 1 of 11
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanNOS2P1645740nitric oxide synthase 2 pseudogene 1
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanMYAS1246750Myasthenia gravis with thymus hyperplasia
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanC10orf27219793
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanNOS2P2201288nitric oxide synthase 2 pseudogene 2
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanIL23R149233interleukin 23 receptor
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanADAMTS14140766ADAM metallopeptidase with thrombospondin type 1 motif, 14
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanOLIG1116448oligodendrocyte transcription factor 1
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanKCNH790134potassium voltage-gated channel, subfamily H (eag-related), member 7
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanLINGO184894leucine rich repeat and Ig domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanHAVCR284868hepatitis A virus cellular receptor 2
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanCD27680381CD276 molecule
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanNOD264127nucleotide-binding oligomerization domain containing 2
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanRTN457142reticulon 4
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanTNFRSF1955504tumor necrosis factor receptor superfamily, member 19
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanXAF154739XIAP associated factor 1
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanTLR954106toll-like receptor 9
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanIL23A51561interleukin 23, alpha subunit p19
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanFOXP350943forkhead box P3
INFERRED, Score=800, UMLKSK CUI: C0751871
HumanICOS29851inducible T-cell co-stimulator
INFERRED, Score=800, UMLKSK CUI: C0751871
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0751871Autoimmune Diseases of the Nervous System0self