OBO ID: DOID:4624
Term Name: Ollier disease Search Ontology:
Synonyms:
  • DYSCHONDROPLASIA
  • Enchondromatosis with haemangiomata
  • ENCHONDROMATOSIS, MULTIPLE
  • Kast's syndrome
  • OSTEOCHONDROMATOSIS
Definition: A syndrome that is characterized by an asymmetric distribution of cartilagenous tumors, which may lead to skeletal deformities and limb-length discrepancy. This condition primarily affects the long bones and cartilage of the joints of the arms and legs, specifically the area where the shaft and head of a long bone meet. (2)
References:
  • GARD:7251
  • ICD10CM:Q78.4
  • MESH:D004687
  • NCI:C3213
  • OMIM:166000
  • ORDO:296
  • SNOMEDCT_US_2023_03_01:46041001
  • UMLS_CUI:C0024454
Ontology: Human Disease   ( DOID:4624 )
Relationships
is a type of:
OTHER Ollier disease PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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