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Details
Link-It Detail - Disease - Demyelinating Autoimmune Diseases, CNS
Debug Stats
  • ### Total Build Time: 211 ms 41.123 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 436 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 449 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=85 ms Completed: 85 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= 1.423 KB
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 3.185 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 6.705 KB
  • CONCEPT_RELATIONSHIPS gt=44 ms Completed: 44 ms rowSize= 9.357 KB
  • CONCEPT_GENES gt=62 ms Completed: 62 ms rowSize= 18.206 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Demyelinating Autoimmune Diseases, CNS C0751873
AUTOIMMUNE DEMYELINATING DIS CNS
Definition (1)
Conditions characterized by loss or dysfunction of myelin (see MYELIN SHEATH) in the brain, spinal cord, or optic nerves secondary to autoimmune mediated processes. This may take the form of a humoral or cellular immune response directed toward myelin or OLIGODENDROGLIA associated autoantigens.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Leukoencephalopathies C0270612
img Autoimmune Diseases of the Nervous System C0751871
img Demyelinating Diseases C0011303
Children (7)
img Diffuse Cerebral Sclerosis of Schilder C0007795
img Encephalomyelitis, Acute Disseminated C0014059
img Myelitis, Transverse C0026976
img Leukoencephalitis, Acute Hemorrhagic C0014077
img Multiple Sclerosis C0026769
img Neuromyelitis Optica C0027873
img Encephalomyelitis, Autoimmune, Experimental C0014072
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076824img Leukoencephalopathies C0270612
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Leukoencephalopathies C0270612
img Immune System Diseases C0021053img Autoimmune Diseases C00043644img Autoimmune Diseases of the Nervous System C0751871
img Nervous System Diseases C0027765img Autoimmune Diseases of the Nervous System C07518713img Autoimmune Diseases of the Nervous System C0751871
img Nervous System Diseases C0027765img Demyelinating Diseases C00113033img Demyelinating Diseases C0011303
Relationships (23)

Relation Types:
diso_​to_​anat : 8
diso_​to_​chem : 4
diso_​to_​diso : 9
diso_​to_​phen : 2


Relationships:
none : 22
entry_​version_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM11img Abs - Autoantibodies C0004358
DISO_to_CHEM11img Autoantibodies C0004358
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_ANAT7img Oligodendroglia C0028944
DISO_to_DISO7img chemically induced C0007994
DISO_to_DISO6img Complication Aspects C1171258
DISO_to_DISO6img Inflammation C0021368
DISO_to_ANAT5img Brain C0006104
DISO_to_ANAT5img Central Nervous System C0927232
DISO_to_ANAT5img In Blood C0005768
DISO_to_ANAT5img Myelin Sheath C0026973
DISO_to_CHEM5img Aquaporin 4 C0292777
DISO_to_DISO5img Multiple Sclerosis C0026769
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_ANAT4img Central Nervous System C0927232
DISO_to_ANAT4img Microglia C0206116
DISO_to_ANAT4img Oligodendrocyte C0028944
DISO_to_CHEM4img Nerve Tissue Proteins C0027759
DISO_to_DISO4img Cardiovirus Infections C0206617
DISO_to_DISO4img Encephalomyelitis, Autoimmune, Experimental C0014072
DISO_to_DISO4img Polyradiculoneuropathy C0032587
DISO_to_DISO4img chemically induced C0007994
DISO_to_DISOentry_version_ofimg AUTOIMMUNE DEMYELINATING DIS CNS C0751873
Genes (242)

Species:
human : 242
Page Size
Current 25
  Page 1 of 10
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanNOS2P1645740nitric oxide synthase 2 pseudogene 1
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanC10orf27219793
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanNOS2P2201288nitric oxide synthase 2 pseudogene 2
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanIL23R149233interleukin 23 receptor
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanADAMTS14140766ADAM metallopeptidase with thrombospondin type 1 motif, 14
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanOLIG1116448oligodendrocyte transcription factor 1
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanKCNH790134potassium voltage-gated channel, subfamily H (eag-related), member 7
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanLINGO184894leucine rich repeat and Ig domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanHAVCR284868hepatitis A virus cellular receptor 2
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanNOD264127nucleotide-binding oligomerization domain containing 2
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanRTN457142reticulon 4
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanTNFRSF1955504tumor necrosis factor receptor superfamily, member 19
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanXAF154739XIAP associated factor 1
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanTLR954106toll-like receptor 9
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanIL23A51561interleukin 23, alpha subunit p19
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanFOXP350943forkhead box P3
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanICOS29851inducible T-cell co-stimulator
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanTRBV5-228613
INFERRED, Score=800, UMLKSK CUI: C0751873
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
INFERRED, Score=800, UMLKSK CUI: C0751873
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0751873Demyelinating Autoimmune Diseases, CNS0self