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Details
Link-It Detail - Disease - Hyperkinesis
Debug Stats
  • ### Total Build Time: 153 ms 43.433 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 272 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 547 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 4.071 KB
  • CONCEPT_RELATIONSHIPS gt=72 ms Completed: 72 ms rowSize= 13.034 KB
  • CONCEPT_GENES gt=49 ms Completed: 49 ms rowSize= 23.852 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperkinesis C0424295
Definition (1)
Excessive movement of muscles of the body as a whole, which may be associated with organic or psychological disorders.
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Dyskinesias C0013384
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Dyskinesias C0013384
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Dyskinesias C0013384
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Dyskinesias C0013384
Relationships (61)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 24
diso_​to_​diso : 23
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 49
isa : 1
mapped_​to : 9
permuted_​term_​of : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO97img chemically induced C0007994
DISO_to_DISO89img chemically induced C0007994
DISO_to_DISO38img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_PHEN37img genetic aspects C0017399
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_PHEN23img genetic aspects C0017399
DISO_to_CHEM18img Central Nervous System Stimulants C0002763
DISO_to_CHEM14img Antipsychotic Agents C0040615
DISO_to_ANAT13img Brain C0006104
DISO_to_CHEM12img Dopamine C0013030
DISO_to_DISO12img Movement Disorders C0026650
DISO_to_CHEM11img Central Nervous System Stimulants C0002763
DISO_to_ANAT10img Prefrontal Cortex C0162783
DISO_to_CHEM10img Amphetamine C0002658
DISO_to_CHEM10img Dopamine C0013030
DISO_to_CHEM10img Serotonin C0036751
DISO_to_PHYS10img Attention C0004268
DISO_to_ANAT9img Hippocampus C0019564
DISO_to_CHEM9img Cocaine C0009170
DISO_to_CHEM9img Serotonin C0036751
DISO_to_DISO9img Anorexia Nervosa C0003125
DISO_to_DISO9img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO9img DELAYED EFF PRENATAL EXPOSURE C0033054
DISO_to_ANAT8img Accumbens nucleus C0028633
DISO_to_CHEM8img Agents, Food Coloring C0016461
Genes (39)

Species:
human : 39
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanADHD4450090Attention deficit-hyperactivity disorder, susceptibility to, 4
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanADHD3450089Attention deficit-hyperactivity disorder, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanADHD2450088Attention deficit-hyperactivity disorder, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanADHD1450087Attention deficit-hyperactivity disorder, susceptibility to, 1
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanGRDX117189Graves disease, susceptibility to, X-linked
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanPANK280025pantothenate kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanIFIH164135interferon induced with helicase C domain 1
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanCC2D1A54862coiled-coil and C2 domain containing 1A
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanGRD250976Graves disease, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanRAI110743retinoic acid induced 1
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanCUL4B8450cullin 4B
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanALDH5A17915aldehyde dehydrogenase 5 family, member A1
img OMIM, Score=1000, UMLKSK CUI: C0424295
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanTSHR7253thyroid stimulating hormone receptor
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanSLC6A36531solute carrier family 6 (neurotransmitter transporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanSGSH6448N-sulfoglucosamine sulfohydrolase
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanPSAP5660prosaposin
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanPRODH5625proline dehydrogenase (oxidase) 1
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanOPHN14983oligophrenin 1
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanNBN4683nibrin
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanNAGLU4669N-acetylglucosaminidase, alpha
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanMANBA4126mannosidase, beta A, lysosomal
img OMIM, Score=1000, UMLKSK CUI: C0424295
HumanKRT53852keratin 5
img OMIM, Score=790, UMLKSK CUI: C0424295
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
img OMIM, Score=1000, UMLKSK CUI: C0424295
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0424295Hyperkinesis0self