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Details
Link-It Detail - Disease - Chromosome Breakage
Debug Stats
  • ### Total Build Time: 37 ms 22.299 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 313 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_TEXT gt=NONE 1 ms Completed: 1 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 198 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 558 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.532 KB
  • CONCEPT_RELATIONSHIPS gt=21 ms Completed: 21 ms rowSize= 12.863 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 5.343 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Chromosome Breakage C0376628
Definition (1)
A type of chromosomal aberration involving DNA BREAKS. Chromosome breakage can result in CHROMOSOMAL TRANSLOCATION; CHROMOSOME INVERSION; or SEQUENCE DELETION.
Semantic Types (1)
Cell or Molecular Dysfunction (T049)
Parents (1)
img Chromosome Aberrations C0008625
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306604img Chromosome Aberrations C0008625
Relationships (52)

Relation Types:
diso_​to_​anat : 12
diso_​to_​chem : 10
diso_​to_​diso : 19
diso_​to_​gene : 1
diso_​to_​phen : 3
diso_​to_​phys : 7


Relationships:
none : 50
mapped_​to : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN127img genetic aspects C0017399
DISO_to_DISO57img Chromosomal translocation C0040715
DISO_to_DISO44img Chromosomal translocation C0040715
DISO_to_PHYS35img DNA Damage Repair C0012899
DISO_to_CHEM22img Binding Protein, DNA C0012940
DISO_to_ANAT20img Chromosome, Human C0008643
DISO_to_CHEM19img DNA C0012854
DISO_to_PHYS19img DNA Damage Repair C0012899
DISO_to_DISO15img Abnormalities, Multiple C0000772
DISO_to_DISO15img Chromosome Aberrations C0008625
DISO_to_PHYS15img DNA Recombination C0034865
DISO_to_ANAT14img Telomere C0085187
DISO_to_CHEM14img Binding Protein, DNA C0012940
DISO_to_CHEM14img Nuclear Proteins C0028589
DISO_to_DISO14img Break, Double-Strand DNA C1511667
DISO_to_DISO14img Chromosome Deletion C0008628
DISO_to_DISO14img DNA Damage C0012860
DISO_to_ANAT13img 1 chromosome C0008651
DISO_to_DISO13img Chromosome Deletion C0008628
DISO_to_DISO12img Chromosome Disorders C0008626
DISO_to_DISO12img Chromosome Inversion C0021943
DISO_to_DISO12img DNA Damage C0012860
DISO_to_DISO12img Neoplasms C0027651
DISO_to_CHEM11img Cell Cycle Protein C0243021
DISO_to_ANAT10img Chromosomes C0008633
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanMDC19656mediator of DNA-damage checkpoint 1
img GENERIF, Score=1000, Pubmed Id: 18411307, UMLKSK CUI: C0376628
HumanPMM25373phosphomannomutase 2
img GENERIF, Score=1000, Pubmed Id: 11891694, UMLKSK CUI: C0376628
HumanHOXA113207homeobox A11
img OMIM, Score=1000, UMLKSK CUI: C0376628
HumanFHIT2272fragile histidine triad
img GENERIF, Score=1000, Pubmed Id: 12007194, UMLKSK CUI: C0376628
HumanFANCA2175Fanconi anemia, complementation group A
img OMIM, Score=1000, UMLKSK CUI: C0376628
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0376628Chromosome Breakage0self