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Details
Link-It Detail - Disease - Legg-Calve-Perthes Disease
Debug Stats
  • ### Total Build Time: 33 ms 21.240 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 350 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 277 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 2.799 KB
  • CONCEPT_RELATIONSHIPS gt=4 ms Completed: 4 ms rowSize= 7.836 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 8.072 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Legg-Calve-Perthes Disease C0023234
Definition (1)
A very rare disorder of unknown etiology affecting children. It is characterized by avascular necrosis of the femoral head.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Femur Head Necrosis C0015814
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Bone Diseases C00059405img Femur Head Necrosis C0015814
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306606img Femur Head Necrosis C0015814
Relationships (17)

Relation Types:
diso_​to_​anat : 10
diso_​to_​diso : 7


Relationships:
none : 12
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
mapped_​to : 1
permuted_​term_​of : 1
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT40img Femur Head C0015813
DISO_to_ANAT34img Hip Joint C0019558
DISO_to_ANAT29img Femur Head C0015813
DISO_to_DISO26img Complication Aspects C1171258
DISO_to_DISO22img Complication Aspects C1171258
DISO_to_ANAT19img Hip Joint C0019558
DISO_to_ANAT17img Femur C0015811
DISO_to_ANAT15img Acetabulum C0000962
DISO_to_ANAT12img Acetabulum C0000962
DISO_to_DISO11img Hip Dislocation, Congenital C0019555
DISO_to_ANAT10img Femur C0015811
DISO_to_DISO10img Osteoarthritis of hip C0029410
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_DISOmapped_toimg Garret Tripp syndrome C2930965
DISO_to_DISOpermuted_term_ofimg Legg-Calve-Perthes Disease C0023234
DISO_to_DISOused_forimg Osteochondritis C0029420
Genes (5)

Species:
human : 5
SpeciesGeneGeneIdGene NameEvidence
HumanTRPS17227trichorhinophalangeal syndrome I
img OMIM, Score=1000, UMLKSK CUI: C0023234
img OMIM, Score=1000, UMLKSK CUI: C0023234
HumanFGB2244fibrinogen beta chain
img GAD, Score=1000, Pubmed Id: 14629463, UMLKSK CUI: C0023234
img GENERIF, Score=923, Pubmed Id: 14629463, UMLKSK CUI: C0023234
HumanF52153coagulation factor V (proaccelerin, labile factor)
img GAD, Score=1000, Pubmed Id: 15125132, UMLKSK CUI: C0023234
HumanEXT12131exostosin glycosyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0023234
HumanCOL2A11280collagen, type II, alpha 1
img GENERIF, Score=1000, Pubmed Id: 17394019, UMLKSK CUI: C0023234
img GENERIF, Score=913, Pubmed Id: 18512791, UMLKSK CUI: C0023234
img OMIM, Score=1000, UMLKSK CUI: C0023234
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023234Legg-Calve-Perthes Disease0self