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Details
Link-It Detail - Disease - CTCV - Congenital talipes calcaneovalgus
Debug Stats
  • ### Total Build Time: 46 ms 9.373 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=26 ms Completed: 26 ms rowSize= 4.719 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 3.041 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
CTCV - Congenital talipes calcaneovalgus C0152237
Relationships (9)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 7


Relationships:
associated_​with : 2
classifies : 2
location_​of : 2
mapped_​to : 3
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATlocation_ofimg Heel C0018870
DISO_to_ANATlocation_ofimg Toes C0040357
DISO_to_DISOclassifiesimg All other congenital anomalies C0810365
DISO_to_DISOmapped_toimg CTCV - Congenital talipes calcaneovalgus C0152237
DISO_to_DISOmapped_toimg Calcaneovalgus deformity of foot C0576228
DISO_to_DISOassociated_withimg Congenital turning outward C0332954
DISO_to_DISOassociated_withimg Congenital turning upward C0332956
DISO_to_DISOmapped_toimg Fixed calcaneovalgus C0426921
DISO_to_DISOclassifiesimg Other and unspecified congenital anomalies C0158795
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanDHCR717177-dehydrocholesterol reductase
img OMIM, Score=1000, UMLKSK CUI: C0152237
HumanCHRNG1146cholinergic receptor, nicotinic, gamma (muscle)
img OMIM, Score=1000, UMLKSK CUI: C0152237
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
img OMIM, Score=1000, UMLKSK CUI: C0152237
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0152237CTCV - Congenital talipes calcaneovalgus0self