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Details
Link-It Detail - Disease - Psychomotor Disorders
Debug Stats
  • ### Total Build Time: 137 ms 37.798 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 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=1 ms Completed: 1 ms rowSize= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=17 ms Completed: 17 ms rowSize= 566 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 985 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.135 KB
  • CONCEPT_RELATIONSHIPS gt=60 ms Completed: 60 ms rowSize= 12.901 KB
  • CONCEPT_GENES gt=37 ms Completed: 37 ms rowSize= 17.287 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Psychomotor Disorders C0033922
Definition (1)
Abnormalities of motor function that are associated with organic and non-organic cognitive disorders.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Neurobehavioral Manifestations C0525041
Children (2)
img Psychomotor Agitation C0085631
img Apraxias C0003635
Ancestral Roots
RootRoot Plus OneDepthParent
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 (77)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 1
diso_​to_​diso : 58
diso_​to_​phen : 2
diso_​to_​phys : 11


Relationships:
none : 69
entry_​version_​of : 1
mapped_​to : 7
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO48img chemically induced C0007994
DISO_to_PHEN43img genetic aspects C0017399
DISO_to_DISO40img Cognition Disorders C0009241
DISO_to_DISO39img Developmental Disabilities C0008073
DISO_to_DISO36img Cognition Disorders C0009241
DISO_to_PHEN36img genetic aspects C0017399
DISO_to_DISO32img Developmental Disabilities C0008073
DISO_to_DISO30img Complication Aspects C1171258
DISO_to_DISO27img chemically induced C0007994
DISO_to_DISO25img Schizophrenia C0036341
DISO_to_PHYS22img Performance, Psychomotor C0033923
DISO_to_DISO20img Intellectual Disability C0025362
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_ANAT18img Brain C0006104
DISO_to_DISO17img Cerebral Palsy C0007789
DISO_to_PHYS16img CHILDHOOD DEVELOPMENT C0008071
DISO_to_PHYS16img Motor Skill C0026612
DISO_to_ANAT14img Brain C0006104
DISO_to_DISO14img Intellectual Disability C0025362
DISO_to_DISO14img Schizophrenia C0036341
DISO_to_PHYS14img Performance, Psychomotor C0033923
DISO_to_DISO13img Depressive Disorder, Major C1269683
DISO_to_DISO13img INFANT PREMATURE DIS C0021295
DISO_to_DISO13img Motor Skills Disorders C0026613
DISO_to_PHYS13img Aging C0001811
Genes (34)

Species:
human : 34
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNHLRC1378884NHL repeat containing 1
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanTSEN54283989TSEN54 tRNA splicing endonuclease subunit
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanFOXP293986forkhead box P2
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanPANK280025pantothenate kinase 2
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanTREM254209triggering receptor expressed on myeloid cells 2
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanPDE11A50940phosphodiesterase 11A
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanCHMP2B25978charged multivesicular body protein 2B
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanSLC25A1510166solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanHUWE110075HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanKDM5C8242lysine (K)-specific demethylase 5C
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanTBP6908TATA box binding protein
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanSUOX6821sulfite oxidase
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanCDKL56792cyclin-dependent kinase-like 5
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanSPAST6683spastin
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanSLC6A46532solute carrier family 6 (neurotransmitter transporter), member 4
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanPSEN15663presenilin 1
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanPRNP5621prion protein
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanPRKAR1A5573protein kinase, cAMP-dependent, regulatory, type I, alpha
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanPOLG5428polymerase (DNA directed), gamma
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanMRE11A4361MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
INFERRED, Score=800, UMLKSK CUI: C0033922
HumanHTR2A33565-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
INFERRED, Score=800, UMLKSK CUI: C0033922
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0033922Psychomotor Disorders0self