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Details
Link-It Detail - Disease - Communication Disorders
Debug Stats
  • [ From Cache ]
  • ### Total Build Time: 34 ms 36.403 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 352 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= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1,023 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 992 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 5.441 KB
  • CONCEPT_RELATIONSHIPS gt=6 ms Completed: 6 ms rowSize= 8.917 KB
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 18.017 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Communication Disorders C0009460
Definition (1)
Disorders of verbal and nonverbal communication caused by receptive or expressive LANGUAGE DISORDERS, cognitive dysfunction (e.g., MENTAL RETARDATION), psychiatric conditions, and HEARING DISORDERS.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (2)
img Mental Disorders Diagnosed in Childhood C0525040
img Neurobehavioral Manifestations C0525041
Children (2)
img Language Disorders C0023015
img Learning Disorders C0023186
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250403img Mental Disorders Diagnosed in Childhood C0525040
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Neurobehavioral Manifestations C0525041
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Neurobehavioral Manifestations C0525041
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250413img Neurobehavioral Manifestations C0525041
Relationships (22)

Relation Types:
diso_​to_​diso : 22


Relationships:
none : 16
isa : 4
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO39img Autistic Disorder C0004352
DISO_to_DISO30img Autistic Disorder C0004352
DISO_to_DISO29img Cognition Disorders C0009241
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_DISO23img Brain Injuries C0270611
DISO_to_DISO18img Developmental Disabilities C0008073
DISO_to_DISO18img Language Development Disorders C0023014
DISO_to_DISO17img CHILD DEVELOPMENT DIS PERVASIVE C0008074
DISO_to_DISO17img Cognition Disorders C0009241
DISO_to_DISO16img Cerebral Palsy C0007789
DISO_to_DISO15img Complication Aspects C1171258
DISO_to_DISO15img Intellectual Disability C0025362
DISO_to_DISO12img Alzheimer Disease C0002395
DISO_to_DISO11img Cerebrovascular accident C0038454
DISO_to_DISO11img DEFECT SPEECH (NOS) C0037822
DISO_to_DISO11img Schizophrenia C0036341
DISO_to_DISOpermuted_term_ofimg Communication Disorders C0009460
DISO_to_DISOisaimg Conversational disorder C0588404
DISO_to_DISOisaimg Idiopathic stammering C0454540
DISO_to_DISOisaimg Non-organic communication disorder C1960521
DISO_to_DISOmapped_toimg Speech and Communication Disorders C1456703
DISO_to_DISOisaimg Speech and language disorder C0023009
Genes (148)

Species:
human : 148
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPARK12677662Parkinson disease 12 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanDYX8406874dyslexia susceptibility 8
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanPARK10170534Parkinson disease 10 (susceptibility)
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanARX170302aristaless related homeobox
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanDYX1C1161582dyslexia susceptibility 1 candidate 1
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanKCTD7154881potassium channel tetramerization domain containing 7
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanTTBK2146057tau tubulin kinase 2
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanSLITRK1114798SLIT and NTRK-like family, member 1
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanFOXP293986forkhead box P2
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanTMEM6791147transmembrane protein 67
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanFAM126A84668family with sequence similarity 126, member A
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanARL684100ADP-ribosylation factor-like 6
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanCEP29080184centrosomal protein 290kDa
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanPANK280025pantothenate kinase 2
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanBBS1079738Bardet-Biedl syndrome 10
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanSIL164374SIL1 nucleotide exchange factor
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanJPH357338junctophilin 3
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanGJC257165gap junction protein, gamma 2, 47kDa
INFERRED, Score=800, UMLKSK CUI: C0009460
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
INFERRED, Score=800, UMLKSK CUI: C0009460
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0009460Communication Disorders0self