Central Nervous System Desmoid Fibromatosis

Preferred Label : Central Nervous System Desmoid Fibromatosis;

NCIt synonyms : Central Nervous System Desmoid-Type Fibromatosis;

NCIt definition : Intracranial and/or spinal involvement by desmoid fibromatosis.;

Neoplastic status : Undetermined;

NCI Metathesaurus CUI : CL512680;

Details

Origin ID

C129548;

UMLS CUI

C4329628;

Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Excludes anatomical site(s)
- Abdomen [NCIt concept]
- Bone [NCIt concept]
- Lung [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Superficial Lesion [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Fibroblast [NCIt concept]
- Neoplastic Spindle-Shaped Fibroblast [NCIt concept]
disease_has_finding
- Collagenous Stroma Formation [NCIt concept]
- Deep Lesion [NCIt concept]
- Infiltrative Growth Pattern [NCIt concept]
- Locally Aggressive Lesion [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Fibroblast [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
disease_mapped_to_gene
- APC Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Trisomy 20 [NCIt concept]
- Trisomy 8 [NCIt concept]
disease_may_have_molecular_abnormality
- CTNNB1 Gene Mutation [NCIt concept]
- Inactivating APC Gene Mutation [NCIt concept]

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