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Details
Link-It Detail - Disease - Flatfoot
Debug Stats
  • ### Total Build Time: 123 ms 31.395 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 314 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 232 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.504 KB
  • CONCEPT_RELATIONSHIPS gt=37 ms Completed: 37 ms rowSize= 4.234 KB
  • CONCEPT_GENES gt=66 ms Completed: 66 ms rowSize= 23.220 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.143 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Flatfoot C0016202
Definition (1)
A condition in which one or more of the arches of the foot have flattened out.
Semantic Types (1)
Anatomical Abnormality (T190)
Parents (1)
img Foot Deformities C0016506
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Foot Deformities C00165063img Foot Deformities C0016506
Relationships (9)

Relation Types:
diso_​to_​anat : 5
diso_​to_​diso : 4


Relationships:
none : 8
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO40img Acquired Foot Deformities C0016507
DISO_to_DISO30img Acquired Foot Deformities C0016507
DISO_to_ANAT29img Foot C0016504
DISO_to_ANAT28img Bone structure of calcaneum C0006655
DISO_to_DISO26img Dysfunction, Tibialis Posterior C1136154
DISO_to_ANAT24img Foot C0016504
DISO_to_ANAT20img Tarsal Bones C0039316
DISO_to_ANAT19img Bone structure of calcaneum C0006655
DISO_to_DISOpermuted_term_ofimg Flatfoot C0016202
Genes (36)

Species:
human : 36
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBRWD3254065bromodomain and WD repeat domain containing 3
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanSIL164374SIL1 nucleotide exchange factor
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanSALL457167sal-like 4 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanB4GALT711285xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanSEC23A10484Sec23 homolog A (S. cerevisiae)
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanTBX49496T-box 4
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanCRLF19244cytokine receptor-like factor 1
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanGAN8139gigaxonin
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanRAB7A7879RAB7A, member RAS oncogene family
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanALMS17840Alstrom syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanTRPS17227trichorhinophalangeal syndrome I
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanSLC16A26567solute carrier family 16, member 2 (thyroid hormone transporter)
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanRYR16261ryanodine receptor 1 (skeletal)
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanPLOD15351procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanMGAT24247mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanHSPG23339heparan sulfate proteoglycan 2
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanGARS2617glycyl-tRNA synthetase
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanFMR12332fragile X mental retardation 1
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanFLNB2317filamin B, beta
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanFLNA2316filamin A, alpha
img OMIM, Score=1000, UMLKSK CUI: C0016202
HumanFBN12200fibrillin 1
img OMIM, Score=1000, UMLKSK CUI: C0016202
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016202Flatfoot0self