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Details
Link-It Detail - Disease - Hyperostosis
Debug Stats
  • ### Total Build Time: 272 ms 35.335 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 199 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 549 bytes
  • CONCEPT_CHILDREN gt=18 ms Completed: 18 ms rowSize= 2.306 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.498 KB
  • CONCEPT_RELATIONSHIPS gt=205 ms Completed: 205 ms rowSize= 13.036 KB
  • CONCEPT_GENES gt=33 ms Completed: 33 ms rowSize= 16.093 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperostosis C0020492
Definition (1)
Increase in the mass of bone per unit volume.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Bone Diseases C0005940
Children (5)
img Exostoses C1442903
img Hyperostosis, Cortical, Congenital C0020497
img Hyperostosis Frontalis Interna C0020494
img Hyperostosis, Sternocostoclavicular C0020499
img Hyperostosis, Diffuse Idiopathic Skeletal C0020498
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Bone Diseases C00059403img Bone Diseases C0005940
Relationships (50)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 1
diso_​to_​diso : 40
diso_​to_​phen : 2


Relationships:
none : 17
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 26
mapped_​to : 4
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO20img Complication Aspects C1171258
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_ANAT10img Bone structure of cranium C0037303
DISO_to_PHEN10img genetic aspects C0017399
DISO_to_DISO9img Meningioma C0025286
DISO_to_DISO8img Meningeal Neoplasms C0025284
DISO_to_DISO7img BONE DEVELOPMENT DISORDER C0005941
DISO_to_ANAT6img Turbinates C1266928
DISO_to_ANAT5img Bone and Bones C0005931
DISO_to_ANAT5img Cervical Vertebrae C0728985
DISO_to_ANAT5img Skull C0037303
DISO_to_CHEM5img Bone Morphogenetic Proteins C0053932
DISO_to_DISO5img Mandibular Diseases C0024689
DISO_to_DISO5img Nasal Obstruction C0027429
DISO_to_DISO5img Osteitis C0029400
DISO_to_DISO5img Spinal Diseases C0037933
DISO_to_ANATis_associated_anatomic_site_ofimg Connective and Soft Tissue C1516798
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skeletal bone C0262950
DISO_to_DISOisaimg 714-715 HYPERTROPHIES OF BONE AND CARTILAGE C0333968
DISO_to_DISOisaimg ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSIS C0020498
DISO_to_DISOpermuted_term_ofimg Bone Hypertrophies C0020492
DISO_to_DISOisaimg Bone island C0265512
DISO_to_DISOisaimg Calcaneal Spur C0158322
DISO_to_DISOmapped_toimg Calvarial hyperostosis C1863351
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanSOST50964sclerostin
img OMIM, Score=833, UMLKSK CUI: C0020492
img OMIM, Score=833, UMLKSK CUI: C0020492
img OMIM, Score=833, UMLKSK CUI: C0020492
img OMIM, Score=833, UMLKSK CUI: C0020492
HumanKL9365klotho
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanTNFSF118600tumor necrosis factor (ligand) superfamily, member 11
img OMIM, Score=833, UMLKSK CUI: C0020492
HumanFGF238074fibroblast growth factor 23
img GENERIF, Score=660, Pubmed Id: 17129170, UMLKSK CUI: C0020492
HumanALMS17840Alstrom syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanTRPS17227trichorhinophalangeal syndrome I
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanCCL26347chemokine (C-C motif) ligand 2
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanPTH1R5745parathyroid hormone 1 receptor
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanPTEN5728phosphatase and tensin homolog
img OMIM, Score=1000, UMLKSK CUI: C0020492
HumanMATN34148matrilin 3
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanHSPG23339heparan sulfate proteoglycan 2
img OMIM, Score=847, UMLKSK CUI: C0020492
HumanHGF3082hepatocyte growth factor (hepapoietin A; scatter factor)
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanEXT22132exostosin glycosyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanEXT12131exostosin glycosyltransferase 1
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanESR12099estrogen receptor 1
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanCOL1A11277collagen, type I, alpha 1
INFERRED, Score=800, UMLKSK CUI: C0020492
HumanCA2760carbonic anhydrase II
img OMIM, Score=833, UMLKSK CUI: C0020492
HumanALPL249alkaline phosphatase, liver/bone/kidney
img GENERIF, Score=1000, Pubmed Id: 12788869, UMLKSK CUI: C0020492
HumanADH1B125alcohol dehydrogenase 1B (class I), beta polypeptide
INFERRED, Score=800, UMLKSK CUI: C0020492
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020492Hyperostosis0self