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Details
Link-It Detail - Disease - Developmental Disabilities
Debug Stats
  • ### Total Build Time: 334 ms 22.148 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 350 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 336 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=10 ms Completed: 10 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 1.541 KB
  • CONCEPT_RELATIONSHIPS gt=268 ms Completed: 268 ms rowSize= 14.083 KB
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 3.901 KB
  • CONCEPT_XREFS gt=17 ms Completed: 17 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Developmental Disabilities C0008073
Definition (1)
A disorder diagnosed in childhood that is marked by either physical or mental impairment or both, which in turn affects the child from achieving age related developmental milestones.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Mental Disorders Diagnosed in Childhood C0525040
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250403img Mental Disorders Diagnosed in Childhood C0525040
Relationships (180)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 1
diso_​to_​diso : 144
diso_​to_​phen : 2
diso_​to_​phys : 23


Relationships:
none : 129
associated_​with : 1
entry_​version_​of : 1
isa : 20
mapped_​to : 18
related_​to : 10
used_​for : 1
Page Size
Current 25
  Page 1 of 8
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN436img genetic aspects C0017399
DISO_to_DISO279img Intellectual Disability C0025362
DISO_to_PHYS258img CHILDHOOD DEVELOPMENT C0008071
DISO_to_DISO246img Complication Aspects C1171258
DISO_to_PHEN192img genetic aspects C0017399
DISO_to_DISO152img Cognition Disorders C0009241
DISO_to_DISO142img Autistic Disorder C0004352
DISO_to_DISO140img Intellectual Disability C0025362
DISO_to_DISO127img Behavior Disorders, Child C0008066
DISO_to_ANAT118img Brain C0006104
DISO_to_DISO109img Complication Aspects C1171258
DISO_to_DISO106img INFANT PREMATURE DIS C0021295
DISO_to_DISO94img Cerebral Palsy C0007789
DISO_to_DISO93img Abnormalities, Multiple C0000772
DISO_to_ANAT89img Brain C0006104
DISO_to_DISO89img Abnormalities, Multiple C0000772
DISO_to_DISO88img Child Behavior Disorders C0008066
DISO_to_DISO85img INFANT VLBW C0282667
DISO_to_DISO85img Mental Disorders C0004936
DISO_to_PHYS85img CHILDHOOD DEVELOPMENT C0008071
DISO_to_DISO82img Cognition Disorders C0009241
DISO_to_DISO81img Nervous System Diseases C0027765
DISO_to_DISO74img Developmental disorder of motor function C0026613
DISO_to_DISO73img chemically induced C0007994
DISO_to_DISO72img Chromosome Deletion C0008628
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanAP3M210947adaptor-related protein complex 3, mu 2 subunit
img GENERIF, Score=861, Pubmed Id: 17293072, UMLKSK CUI: C0008073
HumanZEB29839zinc finger E-box binding homeobox 2
img GENERIF, Score=901, Pubmed Id: 11592033, UMLKSK CUI: C0008073
HumanKCNC33748potassium voltage-gated channel, Shaw-related subfamily, member 3
img GENERIF, Score=1000, Pubmed Id: 16501573, UMLKSK CUI: C0008073
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0008073Developmental Disabilities0self