Pharyngeal Mucosal Melanoma

Preferred Label : Pharyngeal Mucosal Melanoma;

NCIt synonyms : Pharyngeal Melanoma;

NCIt definition : A melanoma that arises from the mucosal surface of the pharynx.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1648022;

Détails

Origin ID

C178521;

UMLS CUI

C5555104;

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
- Head and Neck [NCIt concept]
- Neck [NCIt concept]
- Pharynx [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]
disease_has_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Melanocyte [NCIt concept]
disease_has_normal_tissue_origin
- Mucosa [NCIt concept]
disease_has_primary_anatomic_site
- Head and Neck [NCIt concept]
- Pharynx [NCIt concept]
disease_may_have_molecular_abnormality
- ATRX Gene Mutation [NCIt concept]
- BRAF Gene Mutation [NCIt concept]
- CCND1 Gene Amplification [NCIt concept]
- CDK4 Gene Amplification [NCIt concept]
- CDKN2A Gene Deletion [NCIt concept]
- CDKN2A Gene Mutation [NCIt concept]
- KIT Gene Mutation [NCIt concept]
- MDM2 Gene Amplification [NCIt concept]
- NF1 Gene Deletion [NCIt concept]
- NF1 Gene Mutation [NCIt concept]
- NRAS Gene Mutation [NCIt concept]
- PTEN Gene Deletion [NCIt concept]
- PTEN Gene Mutation [NCIt concept]
- SF3B1 Gene Mutation [NCIt concept]
- SPRED1 Gene Mutation [NCIt concept]
- TP53 Gene Mutation [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients