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Details
Link-It Detail - Disease - Bone Diseases
Debug Stats
  • ### Total Build Time: 955 ms 46.517 KB
  • CONCEPT_NAME gt=19 ms Completed: 19 ms rowSize= 324 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 264 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=12 ms Completed: 12 ms rowSize= 560 bytes
  • CONCEPT_CHILDREN gt=45 ms Completed: 45 ms rowSize= 9.083 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.117 KB
  • CONCEPT_RELATIONSHIPS gt=757 ms Completed: 757 ms rowSize= 14.588 KB
  • CONCEPT_GENES gt=117 ms Completed: 117 ms rowSize= 19.249 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Bone Diseases C0005940
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the bones.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Musculoskeletal Diseases C0026857
Children (21)
img Bone Diseases, Endocrine C0005942
img Epiphyses, Slipped C0014571
img Osteochondritis C0029420
img Osteoarthropathy, Secondary Hypertrophic C0029412
img Genu Varum C0544755
img Bone Diseases, Metabolic C0005944
img Osteitis C0029400
img Bone Neoplasms C0005967
img Bone Diseases, Developmental C0005941
img Bone Diseases, Infectious C0005943
img Osteonecrosis C0029445
img Bone Malalignment C0206231
img Spinal Diseases C0037933
img Osteitis Deformans C0029401
img Genu Valgum C0576093
img Eosinophilic Granuloma C0014461
img Osteoarthropathy, Primary Hypertrophic C0029411
img Bone Cysts C0005937
img Bone Resorption C0005974
img Hyperostosis C0020492
img Osteochondrosis C0029429
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C00268572img Musculoskeletal Diseases C0026857
Relationships (253)

Relation Types:
diso_​to_​anat : 19
diso_​to_​chem : 29
diso_​to_​diso : 191
diso_​to_​phen : 2
diso_​to_​phys : 12


Relationships:
none : 98
associated_​with : 2
isa : 118
location_​of : 1
mapped_​to : 18
may_​diagnose : 2
may_​treat : 4
permuted_​term_​of : 1
related_​to : 9
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT153img Bone and Bones C0005931
DISO_to_DISO138img Complication Aspects C1171258
DISO_to_DISO85img Complication Aspects C1171258
DISO_to_ANAT80img BONE BONES C0005931
DISO_to_PHEN68img genetic aspects C0017399
DISO_to_DISO67img Multiple Myeloma C0026764
DISO_to_CHEM64img Diphosphonates C0012544
DISO_to_ANAT59img Bone structure of cranium C0037303
DISO_to_DISO59img Joint Diseases C0022408
DISO_to_DISO57img Arthropathy C0022408
DISO_to_DISO57img chemically induced C0007994
DISO_to_PHEN55img genetic aspects C0017399
DISO_to_CHEM47img Bone Density Conservation Agents C1563726
DISO_to_PHYS41img Bone Regeneration C0005972
DISO_to_PHYS40img Bone Density C0005938
DISO_to_DISO39img Fracture C0016658
DISO_to_DISO38img Bone Neoplasms C0005967
DISO_to_PHYS36img Bone Density C0005938
DISO_to_DISO34img Bone Neoplasms C0005967
DISO_to_DISO33img Kidney Diseases C0022658
DISO_to_DISO32img Multiple Myeloma C0026764
DISO_to_ANAT31img Bone structure of cranium C0037303
DISO_to_CHEM31img Diphosphonates C0012544
DISO_to_DISO31img Kidney Failure, Chronic C0022661
DISO_to_ANAT30img In Blood C0005768
Genes (566)

Species:
human : 566
Page Size
Current 25
  Page 1 of 23
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanBMND8100188854bone mineral density quantiative trait locus 8
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanBMND7100188853bone mineral density quantiative trait locus 7
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanKIR2DS2100132285killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanLOC445341445341
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanGDF6392255growth differentiation factor 6
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanIYD389434iodotyrosine deiodinase
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanSUMF1285362sulfatase modifying factor 1
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanTHSD7A221981thrombospondin, type I, domain containing 7A
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanNEWENTRY192343Record to support submission of GeneRIFs for a gene not in Gene (human; man).
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanIL23R149233interleukin 23 receptor
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanMIPOL1145282mirror-image polydactyly 1
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0005940
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanFGD4121512FYVE, RhoGEF and PH domain containing 4
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanSP7121340Sp7 transcription factor
img GENERIF, Score=901, Pubmed Id: 18829486, UMLKSK CUI: C0005940
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanANTXR2118429anthrax toxin receptor 2
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanC1QTNF3114899C1q and tumor necrosis factor related protein 3
INFERRED, Score=800, UMLKSK CUI: C0005940
HumanCSMD3114788CUB and Sushi multiple domains 3
INFERRED, Score=800, UMLKSK CUI: C0005940
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0005940Bone Diseases0self