Search Ontology:
Human Disease

Ollier disease

Term ID
DOID:4624
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
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Genes Involved
Zebrafish Models
Citations