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Details
Link-It Detail - Disease - Psychotic Disorders
Debug Stats
  • ### Total Build Time: 548 ms 46.658 KB
  • CONCEPT_NAME gt=20 ms Completed: 20 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 340 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=11 ms Completed: 11 ms rowSize= 587 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 566 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=468 ms Completed: 468 ms rowSize= 14.585 KB
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 27.346 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 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)
A mental disorder characterized by personality change, impaired functioning, and loss of touch with reality. It may be a manifestation of schizophrenia, bipolar disorder, or brain tumor.
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 (440)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 267
diso_​to_​diso : 138
diso_​to_​gene : 1
diso_​to_​phen : 4
diso_​to_​phys : 20


Relationships:
none : 135
classifies : 1
isa : 19
mapped_​to : 39
may_​treat : 241
related_​to : 3
use : 2
Page Size
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  Page 1 of 18
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO1278img Schizophrenia C0036341
DISO_to_CHEM790img ANTIPSYCHOTICS 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_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 Depressive Disorder, Major 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 9-50 UNSPECIFIED MOOD DISORDERS C0525045
DISO_to_DISO79img Mental Disorders C0004936
Genes (70)

Species:
human : 70
Page Size
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  Page 1 of 3
Prior Page
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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=694, Pubmed Id: 15211634, UMLKSK CUI: C0033975
img GENERIF, Score=901, Pubmed Id: 17555717, 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