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Details
Link-It Detail - Disease - Neurobehavioral Manifestations
Debug Stats
  • ### Total Build Time: 172 ms 31.213 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 390 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=0 Completed: 0 ms rowSize= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1,011 bytes
  • CONCEPT_CHILDREN gt=17 ms Completed: 17 ms rowSize= 4.360 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.115 KB
  • CONCEPT_RELATIONSHIPS gt=10 ms Completed: 10 ms rowSize= 1.158 KB
  • CONCEPT_GENES gt=123 ms Completed: 123 ms rowSize= 18.490 KB
  • CONCEPT_XREFS gt=11 ms Completed: 11 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Neurobehavioral Manifestations C0525041
Definition (1)
Signs and symptoms of higher cortical dysfunction caused by organic conditions. These include certain behavioral alterations and impairments of skills involved in the acquisition, processing, and utilization of knowledge or information.
Semantic Types (1)
Sign or Symptom (T184)
Parents (2)
img Neurologic Manifestations C0027854
img Behavior and Behavior Mechanisms C0004928
Children (10)
img Lethargy C0023380
img Psychomotor Disorders C0033922
img Perceptual Disorders C0030975
img Consciousness Disorders C0009792
img Apraxias C0003635
img Communication Disorders C0009460
img Memory Disorders C0025261
img Intellectual Disability C0025362
img Catatonia C0007398
img Confusion C0009676
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neurologic Manifestations C00278543img Neurologic Manifestations C0027854
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370884img Neurologic Manifestations C0027854
img Behavior and Behavior Mechanisms C0004928img Signs and Symptoms C00370882img Behavior and Behavior Mechanisms C0004928
Relationships (1)

Relation Types:
diso_​to_​diso : 1


Relationships:
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOpermuted_term_ofimg Cognitive Manifestation C0525041
Genes (740)

Species:
human : 740
Page Size
Current 25
  Page 1 of 30
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanPARK12677662Parkinson disease 12 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanZNF674641339zinc finger protein 674
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanSCZD12619488schizophrenia 12
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanMIR212406994microRNA 212
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanDYX8406874dyslexia susceptibility 8
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanSCZD11404686Schizophrenia susceptibility locus, chromosome 10q-related
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanIYD389434iodotyrosine deiodinase
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanNHLRC1378884NHL repeat containing 1
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanMRX82378484mental retardation, X-linked 82
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanTRIM74378108tripartite motif containing 74
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanKIAA2022340533KIAA2022
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanSNORD115-1338433
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanNKPD1284353NTPase, KAP family P-loop domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanTSEN54283989TSEN54 tRNA splicing endonuclease subunit
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanDAOA267012D-amino acid oxidase activator
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanNPAS4266743neuronal PAS domain protein 4
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanMRX81266678mental retardation, X-linked 81
INFERRED, Score=800, UMLKSK CUI: C0525041
HumanASPM259266asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0525041
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0525041Neurobehavioral Manifestations0self