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Details
Link-It Detail - Disease - Consciousness Disorders
Debug Stats
  • ### Total Build Time: 36 ms 38.462 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 413 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= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.009 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 553 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 5.461 KB
  • CONCEPT_RELATIONSHIPS gt=8 ms Completed: 8 ms rowSize= 11.800 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 17.532 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Consciousness Disorders C0009792
Definition (1)
Organic mental disorders in which there is impairment of the ability to maintain awareness of self and environment and to respond to environmental stimuli. Dysfunction of the cerebral hemispheres or brain stem RETICULAR FORMATION may result in this condition.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (2)
img Delirium, Dementia, Amnestic, Cognitive Disorders C0029227
img Neurobehavioral Manifestations C0525041
Children (1)
img Unconsciousness C0041657
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Delirium, Dementia, Amnestic, Cognitive Disorders C00292273img Delirium, Dementia, Amnestic, Cognitive Disorders C0029227
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Neurobehavioral Manifestations C0525041
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Neurobehavioral Manifestations C0525041
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250413img Neurobehavioral Manifestations C0525041
Relationships (38)

Relation Types:
diso_​to_​anat : 3
diso_​to_​diso : 28
diso_​to_​phys : 7


Relationships:
none : 37
entry_​version_​of : 1
Page Size
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  Page 1 of 2
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT37img Brain C0006104
DISO_to_PHYS35img Conscious C0234421
DISO_to_DISO25img chemically induced C0007994
DISO_to_DISO23img Brain Injuries C0270611
DISO_to_DISO23img chemically induced C0007994
DISO_to_DISO18img Complication Aspects C1171258
DISO_to_DISO15img Brain Injuries C0270611
DISO_to_DISO15img Epilepsy C0014544
DISO_to_PHYS13img Conscious C0234421
DISO_to_ANAT12img Brain C0006104
DISO_to_DISO10img Seizures C0036572
DISO_to_PHYS10img Awareness C0004448
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_DISO8img Cerebrovascular accident C0038454
DISO_to_DISO8img Chronic vegetative state C0242670
DISO_to_DISO8img Cognition Disorders C0009241
DISO_to_DISO7img Chronic vegetative state C0242670
DISO_to_DISO7img Coma C0009421
DISO_to_DISO7img Function Recoveries C0599766
DISO_to_ANAT6img In Blood C0005768
DISO_to_DISO6img COMPL POSTOP C0032787
DISO_to_DISO6img Coma C0009421
DISO_to_DISO5img Headache C0018681
DISO_to_DISO5img Quadriplegia C0034372
DISO_to_PHYS5img Cognition C0009240
Genes (69)

Species:
human : 69
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanNAGS162417N-acetylglutamate synthase
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanALG1084920ALG10, alpha-1,2-glucosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanC20orf779133
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanMCCC156922methylcrotonoyl-CoA carboxylase 1 (alpha)
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanGAL51083galanin/GMAP prepropeptide
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanNDUFAF429078NADH dehydrogenase (ubiquinone) complex I, assembly factor 4
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanTREX111277three prime repair exonuclease 1
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanAIFM19131apoptosis-inducing factor, mitochondrion-associated, 1
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanSLC7A79056solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanKYNU8942kynureninase
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanTNNT27139troponin T type 2 (cardiac)
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanTKT7086transketolase
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanABCC86833ATP-binding cassette, sub-family C (CFTR/MRP), member 8
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanSCN5A6331sodium channel, voltage-gated, type V, alpha subunit
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanRYR26262ryanodine receptor 2 (cardiac)
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanPKP25318plakophilin 2
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanPIK3CG5294phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanPCCB5096propionyl CoA carboxylase, beta polypeptide
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanPCCA5095propionyl CoA carboxylase, alpha polypeptide
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanOXCT150193-oxoacid CoA transferase 1
INFERRED, Score=800, UMLKSK CUI: C0009792
HumanOTC5009ornithine carbamoyltransferase
INFERRED, Score=800, UMLKSK CUI: C0009792
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0009792Consciousness Disorders0self