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Details
Link-It Detail - Disease - Psychotic Disorders
Debug Stats
  • ### Total Build Time: 821 ms 46.814 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 311 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=2 ms Completed: 2 ms rowSize= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=10 ms Completed: 10 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 566 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=724 ms Completed: 724 ms rowSize= 14.770 KB
  • CONCEPT_GENES gt=57 ms Completed: 57 ms rowSize= 27.346 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Psychotic Disorders C0033975
Definition (1)
Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994)
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Schizophrenia and Disorders with Psychotic Features C0525046
Children (1)
img Psychoses, Substance-Induced C0033941
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Schizophrenia and Disorders with Psychotic Features C05250463img Schizophrenia and Disorders with Psychotic Features C0525046
Relationships (448)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 274
diso_​to_​diso : 139
diso_​to_​gene : 1
diso_​to_​phen : 4
diso_​to_​phys : 20


Relationships:
none : 138
classifies : 1
isa : 24
mapped_​to : 35
may_​treat : 245
permuted_​term_​of : 1
related_​to : 2
use : 2
Page Size
Current 25
  Page 1 of 18
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO1278img Schizophrenia C0036341
DISO_to_CHEM790img Antipsychotic Agents C0040615
DISO_to_CHEM758img ANTIPSYCHOTICS C0040615
DISO_to_DISO718img Schizophrenia C0036341
DISO_to_DISO422img Complication Aspects C1171258
DISO_to_PHEN414img genetic aspects C0017399
DISO_to_DISO289img Bipolar Disorder C0005586
DISO_to_DISO266img Complication Aspects C1171258
DISO_to_DISO246img Cognition Disorders C0009241
DISO_to_PHEN194img genetic aspects C0017399
DISO_to_ANAT166img Brain C0006104
DISO_to_DISO153img Bipolar Disorder C0005586
DISO_to_ANAT128img In Blood C0005768
DISO_to_DISO126img Cognition Disorders C0009241
DISO_to_CHEM124img 4H-Pyrido(1,2-a)pyrimidin-4-one, 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)ethyl)-6 ,7,8,9-tetrahydro-2-methyl- C0073393
DISO_to_CHEM124img Risperidone C0073393
DISO_to_CHEM112img 4H-Pyrido(1,2-a)pyrimidin-4-one, 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)ethyl)-6 ,7,8,9-tetrahydro-2-methyl- C0073393
DISO_to_DISO106img Major Depressive Disorder C1269683
DISO_to_DISO105img AODR disorder C0236969
DISO_to_DISO105img Delusions C0011253
DISO_to_DISO100img Hallucinations C0018524
DISO_to_DISO94img Depressive Disorder C0011581
DISO_to_CHEM89img Piperazines C0031958
DISO_to_CHEM88img Benzodiazepines C0005064
DISO_to_DISO79img Mental Disorders C0004936
Genes (70)

Species:
human : 70
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanNHLRC1378884NHL repeat containing 1
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanDAOA267012D-amino acid oxidase activator
img GENERIF, Score=1000, Pubmed Id: 18466879, UMLKSK CUI: C0033975
img GENERIF, Score=1000, Pubmed Id: 15121480, UMLKSK CUI: C0033975
HumanANKK1255239ankyrin repeat and kinase domain containing 1
img GENERIF, Score=861, Pubmed Id: 15542731, UMLKSK CUI: C0033975
HumanSLEH1170682systemic lupus erythematosus with hemolytic anemia 1
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanDTNBP184062dystrobrevin binding protein 1
img GENERIF, Score=901, Pubmed Id: 17555717, UMLKSK CUI: C0033975
img GENERIF, Score=694, Pubmed Id: 15211634, UMLKSK CUI: C0033975
HumanSLEB364695systemic lupus erythematosus susceptibility 3
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanBANK155024B-cell scaffold protein with ankyrin repeats 1
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanGNB1L54584guanine nucleotide binding protein (G protein), beta polypeptide 1-like
img GENERIF, Score=1000, Pubmed Id: 18003636, UMLKSK CUI: C0033975
HumanPDE11A50940phosphodiesterase 11A
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanDISC127185disrupted in schizophrenia 1
img GENERIF, Score=1000, Pubmed Id: 17673452, UMLKSK CUI: C0033975
HumanB3GAT127087beta-1,3-glucuronyltransferase 1 (glucuronosyltransferase P)
img GENERIF, Score=861, Pubmed Id: 12874601, UMLKSK CUI: C0033975
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanZFYVE2623503zinc finger, FYVE domain containing 26
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanVPS13A23230vacuolar protein sorting 13 homolog A (S. cerevisiae)
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanTREX111277three prime repair exonuclease 1
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanNPC210577Niemann-Pick disease, type C2
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanHUWE110075HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanPICK19463protein interacting with PRKCA 1
img GENERIF, Score=861, Pubmed Id: 17606663, UMLKSK CUI: C0033975
HumanITM2B9445integral membrane protein 2B
img OMIM, Score=1000, UMLKSK CUI: C0033975
HumanAIP9049aryl hydrocarbon receptor interacting protein
img OMIM, Score=666, UMLKSK CUI: C0033975
HumanSELENBP18991selenium binding protein 1
img GENERIF, Score=1000, Pubmed Id: 18163446, UMLKSK CUI: C0033975
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
img OMIM, Score=1000, UMLKSK CUI: C0033975
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0033975Psychotic Disorders0self