Maxillofacial Osteochondroma

Preferred Label : Maxillofacial Osteochondroma;

NCIt definition : A rare osteochondroma that arises from a maxillofacial bone.;

Neoplastic status : Benign;

Details

Origin ID

C202260;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Has associated anatomic sites
- Bone [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Head and Neck [NCIt concept]
- Maxillofacial Bone [NCIt concept]
- Musculoskeletal System [NCIt concept]
- Skull [NCIt concept]
disease_excludes_finding
- Atypia [NCIt concept]
- Increased Cellularity Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mitotic Activity [NCIt concept]
- Necrotic Change [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cartilage Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Chondrocyte [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Cartilaginous Differentiation [NCIt concept]
- Indolent Clinical Course [NCIt concept]
disease_has_normal_cell_origin
- Cartilage Cell [NCIt concept]
- Chondrocyte [NCIt concept]
- Connective and Soft Tissue Cell [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Bone [NCIt concept]
- Cartilage [NCIt concept]
- Head and Neck [NCIt concept]
- Maxillofacial Bone [NCIt concept]
- Musculoskeletal System [NCIt concept]
- Skull [NCIt concept]
disease_mapped_to_gene
- EXT1 Gene [NCIt concept]
- EXT2 Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- del(8q24.1) [NCIt concept]
disease_may_have_molecular_abnormality
- EXT1 Gene Mutation [NCIt concept]
- EXT2 Gene Mutation [NCIt concept]

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