Ciliary Body Spindle Cell Type A Melanoma

Preferred Label : Ciliary Body Spindle Cell Type A Melanoma;

NCIt synonyms : Spindle Cell Type A Melanoma of the Ciliary Body; Spindle Cell Type A Melanoma of Ciliary Body;

NCIt definition : A ciliary body melanoma characterized by the presence of malignant spindle-shaped melanocytes with slender nuclei and no visible nucleoli.;

Neoplastic status : Malignant;

Détails

Origin ID

C6864;

UMLS CUI

C1333053;

Automatic exact mappings (from CISMeF team)
- Spindle cell type a malignant melanoma [ICD-11 More detail]
Disease excludes abnormal cell
- Epithelioid Melanoma Cell [NCIt concept]
- Spindle B Melanoma Cell [NCIt concept]
Disease may have findings
- HMB-45-Positive Neoplastic Cells Present [NCIt concept]
- S-100-Positive Neoplastic Cells Present [NCIt concept]
Excludes anatomical site(s)
- Skin [NCIt concept]
Has associated anatomic sites
- Ciliary Body [NCIt concept]
- Eye [NCIt concept]
- Uvea [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Melanoma Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Melanocyte [NCIt concept]
- Spindle A Melanoma Cell [NCIt concept]
- Spindle Melanoma Cell [NCIt concept]
disease_has_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Melanocyte [NCIt concept]
disease_has_primary_anatomic_site
- Ciliary Body [NCIt concept]
- Eye [NCIt concept]
- Uvea [NCIt concept]
disease_mapped_to_gene
- BAP1 Gene [NCIt concept]
- GNA11 Gene [NCIt concept]
- GNAQ Gene [NCIt concept]
disease_may_have_molecular_abnormality
- BAP1 Gene Mutation [NCIt concept]
- CYSLTR2 Gene Mutation [NCIt concept]
- EIF1AX Gene Mutation [NCIt concept]
- GNA11 Gene Mutation [NCIt concept]
- GNAQ Gene Mutation [NCIt concept]
- PLCB4 Gene Mutation [NCIt concept]
- SF3B1 Gene Mutation [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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