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Details
Link-It Detail - Disease - Child Development Disorders, Pervasive
Debug Stats
  • ### Total Build Time: 140 ms 36.149 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 396 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
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 990 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.541 KB
  • CONCEPT_RELATIONSHIPS gt=73 ms Completed: 73 ms rowSize= 12.918 KB
  • CONCEPT_GENES gt=49 ms Completed: 49 ms rowSize= 18.015 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Child Development Disorders, Pervasive C0008074
Definition (1)
Severe distortions in the development of many basic psychological functions that are not normal for any stage in development. These distortions are manifested in sustained social impairment, speech abnormalities, and peculiar motor movements.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Mental Disorders Diagnosed in Childhood C0525040
Children (2)
img Autistic Disorder C0004352
img Asperger Syndrome C0236792
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250403img Mental Disorders Diagnosed in Childhood C0525040
Relationships (57)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 4
diso_​to_​diso : 29
diso_​to_​gene : 1
diso_​to_​phen : 3
diso_​to_​phys : 17


Relationships:
none : 55
entry_​version_​of : 1
mapped_​to : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN272img genetic aspects C0017399
DISO_to_DISO182img Complication Aspects C1171258
DISO_to_DISO121img Autistic Disorder C0004352
DISO_to_ANAT97img Brain C0006104
DISO_to_DISO93img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO71img Intellectual Disability C0025362
DISO_to_DISO56img Asperger Syndrome C0236792
DISO_to_DISO54img Autistic Disorder C0004352
DISO_to_DISO53img Developmental Disabilities C0008073
DISO_to_PHYS47img GENET PREDISPOSITION C0314657
DISO_to_DISO44img Language Development Disorders C0023014
DISO_to_DISO37img Child Behavior Disorders C0008066
DISO_to_PHYS37img Attention C0004268
DISO_to_PHYS35img Cognition C0009240
DISO_to_PHYS33img Pattern Recognition, Visual C0030709
DISO_to_PHYS30img Anxiety C0003467
DISO_to_DISO29img Stereotyped Behavior C0038271
DISO_to_PHYS28img Child Development C0008071
DISO_to_PHYS28img Social Perception C0037427
DISO_to_CHEM27img ANTIPSYCHOTICS C0040615
DISO_to_PHEN27img genetic aspects C0017399
DISO_to_DISO26img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO26img Complication Aspects C1171258
DISO_to_PHYS26img Emotions C0013987
DISO_to_PHYS26img Visual Perception C0042830
Genes (133)

Species:
human : 133
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDAOA267012D-amino acid oxidase activator
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanARX170302aristaless related homeobox
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanDYX1C1161582dyslexia susceptibility 1 candidate 1
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanXIRP2129446xin actin-binding repeat containing 2
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanTPH2121278tryptophan hydroxylase 2
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanAGAP1116987ArfGAP with GTPase domain, ankyrin repeat and PH domain 1
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanFOXP293986forkhead box P2
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanCPA593979carboxypeptidase A5
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanCADPS293664Ca++-dependent secretion activator 2
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanMLPH79083melanophilin
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanWNK365267WNK lysine deficient protein kinase 3
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanNSD164324nuclear receptor binding SET domain protein 1
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanROBO364221roundabout, axon guidance receptor, homolog 3 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanNLGN4X57502neuroligin 4, X-linked
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanATP10A57194ATPase, class V, type 10A
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanPRPF40A55660PRP40 pre-mRNA processing factor 40 homolog A (S. cerevisiae)
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanRBFOX154715RNA binding protein, fox-1 homolog (C. elegans) 1
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanROBO454538roundabout, axon guidance receptor, homolog 4 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanNLGN354413neuroligin 3
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanSNTG254221syntrophin, gamma 2
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanSTK3927347serine threonine kinase 39
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanDISC127185disrupted in schizophrenia 1
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanNBEA26960neurobeachin
INFERRED, Score=800, UMLKSK CUI: C0008074
HumanCOPG226958coatomer protein complex, subunit gamma 2
INFERRED, Score=800, UMLKSK CUI: C0008074
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0008074Child Development Disorders, Pervasive0self