Craniofacial Fibrous Dysplasia

Preferred Label : Craniofacial Fibrous Dysplasia;

NCIt definition : Fibrous dysplasia affecting the craniofacial bones.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL932243;

Details

Origin ID

C173926;

UMLS CUI

C4704742;

Automatic exact mappings (from CISMeF team)
- Craniofacial Fibrous Dysplasia [MeSH Descriptor]
- Craniofacial Fibrous Dysplasia [MeSH concept]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
Has associated anatomic sites
- Bone [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniofacial Fibrous Dysplasia [MeSH Descriptor]
disease_excludes_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Fibrotic Stroma Formation [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Poorly Organized and Inadequately Mineralized Bone Present [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Medullary Bone [NCIt concept]
disease_has_primary_anatomic_site
- Bone [NCIt concept]
- Musculoskeletal System [NCIt concept]
- Skull [NCIt concept]
disease_mapped_to_gene
- GNAS Gene [NCIt concept]
disease_may_have_molecular_abnormality
- GNAS Gene Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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