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Details
Link-It Detail - Disease - Neurotic Disorders
Debug Stats
  • ### Total Build Time: 100 ms 31.935 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 253 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=9 ms Completed: 9 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.102 KB
  • CONCEPT_RELATIONSHIPS gt=60 ms Completed: 60 ms rowSize= 12.429 KB
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 15.908 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Neurotic Disorders C0027932
Definition (1)
class of mental disorders milder than psychosis, including hysteria, fugue, obsession, phobia, etc.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Mental Disorders C0004936
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C00049362img Mental Disorders C0004936
Relationships (63)

Relation Types:
diso_​to_​diso : 48
diso_​to_​phen : 2
diso_​to_​phys : 13


Relationships:
none : 32
entry_​version_​of : 1
isa : 13
mapped_​to : 17
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN45img genetic aspects C0017399
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_PHYS35img Personality C0031208
DISO_to_PHYS24img Extraversion (Psychology) C0015382
DISO_to_DISO23img Complication Aspects C1171258
DISO_to_DISO23img Depression C0011570
DISO_to_PHEN23img genetic aspects C0017399
DISO_to_DISO21img DISORDER PERSONALITY C0031212
DISO_to_DISO19img Depressive Disorder C0011581
DISO_to_DISO19img Life Stress C0038443
DISO_to_DISO16img Depression C0011570
DISO_to_PHYS16img Anxiety C0003467
DISO_to_PHYS16img Emotions C0013987
DISO_to_PHYS16img Personality C0031208
DISO_to_DISO15img Depressive Disorder, Major C1269683
DISO_to_DISO14img DISORDER PERSONALITY C0031212
DISO_to_PHYS14img EXTRAVERSION PSYCHOL C0015382
DISO_to_DISO13img Anxiety Disorders C0003469
DISO_to_DISO13img Depressive Disorder C0011581
DISO_to_DISO12img Somatoform Disorder C0037650
DISO_to_DISO11img Mood Disorders C0525045
DISO_to_PHYS11img Concept, Self C0036594
DISO_to_DISO10img Anxiety Disorders C0003469
DISO_to_DISO10img DIS IN TWINS C0012675
DISO_to_DISO10img Depressive Disorder, Major C1269683
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanDAOA267012D-amino acid oxidase activator
img GENERIF, Score=1000, Pubmed Id: 18346999, UMLKSK CUI: C0027932
HumanANKK1255239ankyrin repeat and kinase domain containing 1
img GENERIF, Score=660, Pubmed Id: 15812318, UMLKSK CUI: C0027932
HumanMDGA2161357MAM domain containing glycosylphosphatidylinositol anchor 2
img GENERIF, Score=1000, Pubmed Id: 18762592, UMLKSK CUI: C0027932
HumanXBP17494X-box binding protein 1
img GENERIF, Score=1000, Pubmed Id: 16154272, UMLKSK CUI: C0027932
HumanSLC6A46532solute carrier family 6 (neurotransmitter transporter), member 4
img GENERIF, Score=694, Pubmed Id: 18188666, UMLKSK CUI: C0027932
img GENERIF, Score=694, Pubmed Id: 14966478, UMLKSK CUI: C0027932
img GENERIF, Score=1000, Pubmed Id: 17216342, UMLKSK CUI: C0027932
img GENERIF, Score=861, Pubmed Id: 12605095, UMLKSK CUI: C0027932
img GENERIF, Score=694, Pubmed Id: 18687577, UMLKSK CUI: C0027932
HumanPDE4D5144phosphodiesterase 4D, cAMP-specific
img GENERIF, Score=1000, Pubmed Id: 18711446, UMLKSK CUI: C0027932
HumanMAOA4128monoamine oxidase A
img GAD, Score=1000, Pubmed Id: 12815746, UMLKSK CUI: C0027932
HumanDRD21813dopamine receptor D2
img GENERIF, Score=660, Pubmed Id: 15812318, UMLKSK CUI: C0027932
HumanCOMT1312catechol-O-methyltransferase
img GAD, Score=1000, Pubmed Id: 12815746, UMLKSK CUI: C0027932
img GENERIF, Score=861, Pubmed Id: 15956988, UMLKSK CUI: C0027932
img GENERIF, Score=1000, Pubmed Id: 18384078, UMLKSK CUI: C0027932
HumanBDNF627brain-derived neurotrophic factor
img GAD, Score=1000, Pubmed Id: 16043130, UMLKSK CUI: C0027932
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0027932Neurotic Disorders0self