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Details
Link-It Detail - Disease - Coxa valga
Debug Stats
  • ### Total Build Time: 12 ms 20.534 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 318 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 289 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= 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=2 ms Completed: 2 ms rowSize= 3.187 KB
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 15.540 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.145 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Coxa valga C0239137
Definition (1)
Hip deformity in which the angle between the femoral neck and its shaft is increased. It may be congenital, acquired, or developmental.
Relationships (6)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 4


Relationships:
none : 5
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT1img Femur C0015811
DISO_to_ANAT1img Fibula C0016068
DISO_to_DISO1img Adolescent Coxa Vara C0149887
DISO_to_DISO1img ECTROMELIA C0013589
DISO_to_DISO1img Lower Extremity Deformities, Congenital C0431943
DISO_to_DISOpermuted_term_ofimg Coxa valga C0239137
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanSIL164374SIL1 nucleotide exchange factor
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanRAB2351715RAB23, member RAS oncogene family
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanB4GALT711285xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanADAMTSL29719ADAMTS-like 2
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanEIF2AK39451eukaryotic translation initiation factor 2-alpha kinase 3
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanMGAT24247mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanHSPG23339heparan sulfate proteoglycan 2
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanGLB12720galactosidase, beta 1
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanGALNS2588galactosamine (N-acetyl)-6-sulfate sulfatase
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanFUCA12517fucosidase, alpha-L- 1, tissue
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanFLNA2316filamin A, alpha
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanERCC52073excision repair cross-complementing rodent repair deficiency, complementation group 5
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanCOL11A11301collagen, type XI, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
img OMIM, Score=1000, UMLKSK CUI: C0239137
HumanATP7A538ATPase, Cu++ transporting, alpha polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0239137
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0239137Coxa valga0self