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Details
Link-It Detail - Disease - Neurodegenerative Diseases
Debug Stats
  • ### Total Build Time: 545 ms 43.741 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 350 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 370 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= 559 bytes
  • CONCEPT_CHILDREN gt=41 ms Completed: 41 ms rowSize= 5.736 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.115 KB
  • CONCEPT_RELATIONSHIPS gt=272 ms Completed: 272 ms rowSize= 14.346 KB
  • CONCEPT_GENES gt=214 ms Completed: 214 ms rowSize= 19.924 KB
  • CONCEPT_XREFS gt=10 ms Completed: 10 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Neurodegenerative Diseases C0524851
Definition (1)
Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Nervous System Diseases C0027765
Children (13)
img Postpoliomyelitis Syndrome C0080040
img Lewy Body Disease C0752347
img Paraneoplastic Syndromes, Nervous System C0751911
img Heredodegenerative Disorders, Nervous System C0751870
img Motor Neuron Disease C0085084
img Olivopontocerebellar Atrophies C0028968
img TDP-43 Proteinopathies C2718017
img Prion Diseases C0162534
img Subacute Combined Degeneration C0221065
img Multiple System Atrophy C0393571
img Tauopathies C0949664
img Parkinson Disease C0030567
img Shy-Drager Syndrome C0037019
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C00277652img Nervous System Diseases C0027765
Relationships (205)

Relation Types:
diso_​to_​anat : 37
diso_​to_​chem : 61
diso_​to_​diso : 71
diso_​to_​gene : 8
diso_​to_​phen : 2
diso_​to_​phys : 26


Relationships:
none : 174
entry_​version_​of : 1
gene_​associated_​with_​disease : 7
gene_​product_​malfunction_​associated_​with_​disease : 3
is_​associated_​anatomic_​site_​of : 2
isa : 12
mapped_​to : 6
Page Size
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  Page 1 of 9
Prior Page
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN598img genetic aspects C0017399
DISO_to_PHEN407img genetic aspects C0017399
DISO_to_ANAT307img Brain C0006104
DISO_to_ANAT236img Brain C0006104
DISO_to_ANAT223img Neurons C0027882
DISO_to_ANAT206img Neurons C0027882
DISO_to_DISO194img Complication Aspects C1171258
DISO_to_CHEM146img Neuroprotective Agents C0242912
DISO_to_PHYS146img Aging C0001811
DISO_to_CHEM123img Agents, Neuroprotective C0242912
DISO_to_DISO115img chemically induced C0007994
DISO_to_DISO107img Complication Aspects C1171258
DISO_to_ANAT106img Mitochondria C0026237
DISO_to_CHEM101img Nerve Tissue Proteins C0027759
DISO_to_DISO100img chemically induced C0007994
DISO_to_PHYS98img Aging C0001811
DISO_to_DISO86img Oxidative Stress C0242606
DISO_to_DISO82img Alzheimer Disease C0002395
DISO_to_DISO81img Oxidative Stress C0242606
DISO_to_DISO80img Neoplasms C0027651
DISO_to_DISO76img Animal Disease Models C0012644
DISO_to_PHYS73img Apoptosis C0162638
DISO_to_DISO72img Dementia C0497327
DISO_to_DISO69img Cognition Disorders C0009241
DISO_to_CHEM65img Peptide C0030956
Genes (1449)

Species:
human : 1449
Page Size
Current 25
  Page 1 of 58
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanFASA100192455fertility associated sperm antigen
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanAD10780912Alzheimer disease-10
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC729225729225
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC647859647859occludin pseudogene
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC646506646506lysosomal-associated membrane protein 1 pseudogene
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC645503645503SUMO-activating enzyme subunit 2-like
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC643387643387TAR DNA binding protein pseudogene
img GENERIF, Score=1000, Pubmed Id: 18091558, UMLKSK CUI: C0524851
img GENERIF, Score=901, Pubmed Id: 17923623, UMLKSK CUI: C0524851
HumanZNF674641339zinc finger protein 674
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanC1orf190541468
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanCLN9497231ceroid-lipofuscinosis, neuronal 9
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanAD9450086Alzheimer disease 9
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanMIR133B442890microRNA 133b
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanCDNF441549cerebral dopamine neurotrophic factor
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanZYG11A440590zyg-11 family member A, cell cycle regulator
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC439999439999
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanMIR212406994microRNA 212
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanMIR146A406938microRNA 146a
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC401495401495
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanHSP90AB2P391634heat shock protein 90kDa alpha (cytosolic), class B member 2, pseudogene
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanSKINTL391037Skint-like, pseudogene
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLDLRAD1388633low density lipoprotein receptor class A domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanLOC388630388630
INFERRED, Score=800, UMLKSK CUI: C0524851
HumanARMS2387715age-related maculopathy susceptibility 2
INFERRED, Score=800, UMLKSK CUI: C0524851
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0524851Neurodegenerative Diseases0self