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Details
Link-It Detail - Disease - Anticipation, Genetic
Debug Stats
  • ### Total Build Time: 21 ms 12.321 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 578 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 1.543 KB
  • CONCEPT_RELATIONSHIPS gt=10 ms Completed: 10 ms rowSize= 7.862 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Anticipation, Genetic C0600498
ANTICIPATION GENET
Definition (1)
A phenomenon in which the signs and symptoms of some genetic conditions tend to become more severe and/or appear at an earlier age as the disorder is passed from one generation to the next. Huntington disease is an example of a genetic disorder in which the biological mechanism for this phenomenon has been well documented. In other cases, it may be due to factors such as increased surveillance or other nongenetic causes.
Semantic Types (1)
Organism Attribute (T032)
Parents (1)
img Genetic Predisposition to Disease C0314657
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306606img Genetic Predisposition to Disease C0314657
Relationships (18)

Relation Types:
phys_​to_​anat : 1
phys_​to_​chem : 1
phys_​to_​diso : 11
phys_​to_​phen : 2
phys_​to_​phys : 3


Relationships:
none : 17
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
PHYS_to_DISO7img Colorectal Neoplasms, Hereditary Nonpolyposis C0009405
PHYS_to_PHEN7img genetic aspects C0017399
PHYS_to_PHEN5img genetic aspects C0017399
PHYS_to_PHYS3img Mutation C0026882
PHYS_to_ANAT2img Brain C0006104
PHYS_to_CHEM2img Telomerase C0087071
PHYS_to_DISO2img Auditory vertigo C0025281
PHYS_to_DISO2img Cancer Syndrome, Hereditary C0027672
PHYS_to_DISO2img Dyskeratosis Congenita C0265965
PHYS_to_DISO2img Expanded Trinucleotide Repeat C0524894
PHYS_to_DISO2img Hodgkin Disease C0019829
PHYS_to_DISO2img Inflammatory Bowel Diseases C0021390
PHYS_to_DISO2img Li-Fraumeni Syndrome C0085390
PHYS_to_DISO2img Pancreatic Neoplasm C0030297
PHYS_to_DISO2img Schizophrenia C0036341
PHYS_to_DISO2img Spastic Paraplegia, Hereditary C0037773
PHYS_to_PHYS2img Mutation C0026882
PHYS_to_PHYSpermuted_term_ofimg ANTICIPATION GENET C0600498
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0600498Anticipation, Genetic0self