Osteofibrous Dysplasia

Preferred Label : Osteofibrous Dysplasia;

NCIt synonyms : Osteofibrous Dysplasia of Bone; OFD; Kempson-Campanacci Lesion; Ossifying Fibroma of Long Bones;

NCIt definition : A benign, usually self-limited fibro-osseous lesion of the bone that affects infants and children. It usually arises from the cortical bone of the anterior mid-shaft of the tibia. Patients usually present with swelling or painless bowing of the tibia. Progression to adamantinoma has been reported in some cases.;

Details

Origin ID

C53970;

UMLS CUI

C1709353;

Automatic exact mappings (from CISMeF team)
- Occipital frontal diameter [LOINC component]
- Orofaciodigital syndrome [ORDO Disease]
- Osteofibrous dysplasia [ORDO Disease]
Currated CISMeF NLP mapping
- Fibrous dysplasia (disorder) [SNOMED CT concept]
- Fibrous dysplasia of bone [MedDRA Preferred Term]
- Fibrous dysplasia of bone [ICD-11 Subcategory]
- Fibrous dysplasia of bone [ORDO Disease]
- Fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- Fibrous dysplasia of the bones [HPO term]
- Osteofibrous dysplasia (disorder) [SNOMED CT concept]
- Osteofibrous dysplasia, susceptibility to [OMIM Phenotype]
- fibrous dysplasia [Radlex concept]
- fibrous dysplasia of bone [MeSH Descriptor]
- fibrous dysplasia of bone [MeSH concept]
- fibrous dysplasia of bone, nos [SNOMED Notion]
- osteofibrous dysplasia [MeSH concept]
- osteofibrous dysplasia [MeSH Supplementary Concept]
Has associated anatomic sites
- Bone [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Osteofibrous dysplasia (disorder) [SNOMED CT concept]
- osteofibrous dysplasia [MeSH Supplementary Concept]
- osteofibrous dysplasia [MeSH concept]
disease_may_have_cytogenetic_abnormality
- Trisomy 12 [NCIt concept]
- Trisomy 7 [NCIt concept]
- Trisomy 8 [NCIt concept]

Keyword's position in hierarchy(ies) :

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