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DO Term : Ollier disease [DOID:4624] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • ICD10CM:Q78.4,
  • SNOMEDCT_US_2023_03_01:46041001,
  • ORDO:296,
  • UMLS_CUI:C0024454,
  • dyschondroplasia,
  • Kast's syndrome,
  • OMIM:166000,
  • Enchondromatosis with haemangiomata,
  • NCI:C3213,
  • GARD:7251,
  • MESH:D004687,
  • 166000,
  • osteochondromatosis,
  • ENCHONDROMATOSIS, MULTIPLE
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Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents