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Details
Link-It Detail - Disease - Foot Deformities
Debug Stats
  • ### Total Build Time: 46 ms 38.742 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 250 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 560 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.672 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.117 KB
  • CONCEPT_RELATIONSHIPS gt=17 ms Completed: 17 ms rowSize= 12.338 KB
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 20.138 KB
  • 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)
Foot Deformities C0016506
Definition (1)
Alterations or deviations from normal shape or size which result in a disfigurement of the foot.
Semantic Types (1)
Anatomical Abnormality (T190)
Parents (1)
img Musculoskeletal Diseases C0026857
Children (6)
img Flatfoot C0016202
img Hallux Varus C0546297
img Foot Deformities, Congenital C0016508
img Hammer Toe Syndrome C1136178
img Foot Deformities, Acquired C0016507
img Hallux Valgus C0018536
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C00268572img Musculoskeletal Diseases C0026857
Relationships (30)

Relation Types:
diso_​to_​anat : 9
diso_​to_​diso : 20
diso_​to_​phen : 1


Relationships:
none : 16
isa : 11
mapped_​to : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT22img Foot C0016504
DISO_to_ANAT21img Foot C0016504
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_DISO19img Disease of foot C0016510
DISO_to_ANAT18img Metatarsal Bones C0025584
DISO_to_DISO18img Complication Aspects C1171258
DISO_to_ANAT17img Ankle Joint C0003087
DISO_to_ANAT16img Bone structure of calcaneum C0006655
DISO_to_ANAT16img Metatarsal Bones C0025584
DISO_to_PHEN11img genetic aspects C0017399
DISO_to_ANAT10img Metatarsophalangeal Joint C0025589
DISO_to_DISO10img Hallux Valgus C0018536
DISO_to_ANAT9img Tarsal Bones C0039316
DISO_to_ANAT9img Toes C0040357
DISO_to_DISO9img Charcot-Marie-Tooth Disease C0007959
DISO_to_DISO9img Disease of foot C0016510
DISO_to_DISOisaimg Adductus deformity of foot C0410773
DISO_to_DISOisaimg Calcaneus deformity of foot C0410766
DISO_to_DISOisaimg Deformity of foot due to rheumatoid arthritis C2317001
DISO_to_DISOisaimg Equinus deformity of foot C0410760
DISO_to_DISOpermuted_term_ofimg Foot Deformities C0016506
DISO_to_DISOmapped_toimg Krauss Herman Holmes syndrome C2931549
DISO_to_DISOmapped_toimg MESOMELIC DYSPLASIA, KANTAPUTRA TYPE C1835009
DISO_to_DISOisaimg Pronated forefoot C0426926
DISO_to_DISOisaimg Pronation deformity of the foot C0410771
Genes (114)

Species:
human : 114
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBRWD3254065bromodomain and WD repeat domain containing 3
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanHYLS1219844hydrolethalus syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanSBF281846SET binding factor 2
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanPANK280025pantothenate kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanSH3TC279628SH3 domain and tetratricopeptide repeats 2
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanSIL164374SIL1 nucleotide exchange factor
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanNSD164324nuclear receptor binding SET domain protein 1
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanPRX57716periaxin
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanPLEKHG557449pleckstrin homology domain containing, family G (with RhoGef domain) member 5
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanSALL457167sal-like 4 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanPEX2655670peroxisomal biogenesis factor 26
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanGDAP154332ganglioside induced differentiation associated protein 1
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanFBXO725793F-box protein 7
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanRAB3GAP225782RAB3 GTPase activating protein subunit 2 (non-catalytic)
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanKIF1B23095kinesin family member 1B
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanCCT522948chaperonin containing TCP1, subunit 5 (epsilon)
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanB4GALT711285xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanSEC23A10484Sec23 homolog A (S. cerevisiae)
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanNDRG110397N-myc downstream regulated 1
img OMIM, Score=1000, UMLKSK CUI: C0016506
HumanALG310195ALG3, alpha-1,3- mannosyltransferase
INFERRED, Score=800, UMLKSK CUI: C0016506
HumanMFN29927mitofusin 2
img OMIM, Score=1000, UMLKSK CUI: C0016506
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016506Foot Deformities0self