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Details
Link-It Detail - Disease - Osteochondromatosis
Debug Stats
  • ### Total Build Time: 227 ms 26.811 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 236 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= 187 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 550 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 568 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=70 ms Completed: 70 ms rowSize= 4.053 KB
  • CONCEPT_RELATIONSHIPS gt=100 ms Completed: 100 ms rowSize= 14.433 KB
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 5.312 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Osteochondromatosis C0206641
Definition (1)
A condition marked by the presence of multiple osteochondromas. (Dorland, 27th ed)
Semantic Types (1)
Neoplastic Process (T191)
Parents (1)
img Osteochondroma C0029423
Children (1)
img Exostoses, Multiple Hereditary C0015306
Ancestral Roots
RootRoot Plus OneDepthParent
img Neoplasms C0027651img Neoplasms by Histologic Type C00276527img Osteochondroma C0029423
img Skin and Connective Tissue Diseases C0175166img Connective Tissue Diseases C00097826img Osteochondroma C0029423
img Musculoskeletal Diseases C0026857img Bone Diseases C00059406img Osteochondroma C0029423
Relationships (28)

Relation Types:
diso_​to_​anat : 15
diso_​to_​diso : 12
diso_​to_​phen : 1


Relationships:
none : 7
is_​abnormal_​cell_​of_​disease : 4
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 3
is_​normal_​cell_​origin_​of_​disease : 4
is_​not_​finding_​of_​disease : 4
is_​not_​normal_​cell_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 2
may_​be_​cytogenetic_​abnormality_​of_​disease : 1
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO8img Bone Neoplasms C0005967
DISO_to_DISO3img Complication Aspects C1171258
DISO_to_ANAT2img Bone structure of radius C0034627
DISO_to_ANAT2img Knee Joint C0022745
DISO_to_ANAT2img Synovial Membrane C0039099
DISO_to_DISO2img Chondromatosis, Synovial C0008476
DISO_to_PHEN2img genetic aspects C0017399
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Cartilage C0007301
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Cartilage Cell C3161470
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Cell of connective tissue C0009781
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Chondrocyte C0225369
DISO_to_ANATis_normal_cell_origin_of_diseaseimg Chondrocytes C0225369
DISO_to_ANATis_associated_anatomic_site_ofimg Connective and Soft Tissue C1516798
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Cartilage Cell C1709167
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Cell C0597032
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Chondrocyte C1513939
DISO_to_ANATis_abnormal_cell_of_diseaseimg Neoplastic Connective and Soft Tissue Cell C1513942
DISO_to_ANATis_not_normal_cell_origin_of_diseaseimg Nerve Cell, Neuroepithelial Cell, and Supporting Cell of the Nervous System C1518293
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skeletal bone C0262950
DISO_to_DISOis_finding_of_diseaseimg Cartilaginous Differentiation C1707309
DISO_to_DISOis_not_finding_of_diseaseimg Increased Cellularity Present C1512694
DISO_to_DISOis_finding_of_diseaseimg Indolent Clinical Course C1334168
DISO_to_DISOis_not_finding_of_diseaseimg Mitotic Activity C1334779
DISO_to_DISOis_finding_of_diseaseimg Multifocal Lesion C1334819
DISO_to_DISOis_not_finding_of_diseaseimg Necrotic changes (finding) C1334928
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanTRPS17227trichorhinophalangeal syndrome I
INFERRED, Score=800, UMLKSK CUI: C0206641
HumanPTH1R5745parathyroid hormone 1 receptor
img OMIM, Score=1000, UMLKSK CUI: C0206641
HumanEXT22132exostosin glycosyltransferase 2
img GENERIF, Score=1000, Pubmed Id: 18373409, UMLKSK CUI: C0206641
img GENERIF, Score=1000, Pubmed Id: 15586175, UMLKSK CUI: C0206641
HumanEXT12131exostosin glycosyltransferase 1
img GENERIF, Score=1000, Pubmed Id: 15586175, UMLKSK CUI: C0206641
img GENERIF, Score=1000, Pubmed Id: 18373409, UMLKSK CUI: C0206641
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0206641Osteochondromatosis0self