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Details
Link-It Detail - Disease - Ring Chromosomes
Debug Stats
  • ### Total Build Time: 18 ms 16.834 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 204 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= 189 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 558 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.532 KB
  • CONCEPT_RELATIONSHIPS gt=7 ms Completed: 7 ms rowSize= 12.821 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Ring Chromosomes C0035639
Definition (1)
Aberrant chromosomes with no ends, i.e., circular.
Semantic Types (1)
Acquired Abnormality (T020)
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 (55)

Relation Types:
anat_​to_​anat : 8
anat_​to_​diso : 45
anat_​to_​phys : 2


Relationships:
none : 18
disease_​may_​have_​cytogenetic_​abnormality : 19
isa : 1
mapped_​to : 16
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
ANAT_to_DISO32img Abnormalities, Multiple C0000772
ANAT_to_PHYS25img Mosaicism C0026578
ANAT_to_PHYS19img Mosaicism C0026578
ANAT_to_DISO14img Abnormalities, Multiple C0000772
ANAT_to_ANAT13img 20 chromosome C0008663
ANAT_to_DISO12img Chromosome Aberrations C0008625
ANAT_to_DISO12img Epilepsy C0014544
ANAT_to_ANAT11img 14 chromosome C0008656
ANAT_to_DISO11img Chromosome Deletion C0008628
ANAT_to_ANAT10img 20 chromosome C0008663
ANAT_to_DISO10img Epilepsy C0014544
ANAT_to_DISO10img Intellectual Disability C0025362
ANAT_to_ANAT9img 22 chromosome C0008665
ANAT_to_DISO9img Intellectual Disability C0025362
ANAT_to_ANAT8img 1 chromosome C0008651
ANAT_to_ANAT8img 7 chromosome C0008670
ANAT_to_ANAT8img Chromosome, Human X C1136735
ANAT_to_DISO8img Chromosome Disorders C0008626
ANAT_to_ANATpermuted_term_ofimg Ring Chromosomes C0035639
ANAT_to_DISOdisease_may_have_cytogenetic_abnormalityimg Atypical Lipoma C1266129
ANAT_to_DISOdisease_may_have_cytogenetic_abnormalityimg Childhood Parosteal Osteogenic Sarcoma C1332994
ANAT_to_DISOisaimg Chromosome 1 ring C1519099
ANAT_to_DISOmapped_toimg Chromosome 10 ring C2931727
ANAT_to_DISOmapped_toimg Chromosome 12 ring C0795843
ANAT_to_DISOmapped_toimg Chromosome 13 ring C2931808
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0035639Ring Chromosomes0self