Cervical Mucoepidermoid Carcinoma

Preferred Label : Cervical Mucoepidermoid Carcinoma;

NCIt definition : A rare carcinoma that arises from the cervix. It is characterized by the presence of squamous cells, mucus producing cells, and cells of intermediate type.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL1663490;

Details

Origin ID

C180878;

UMLS CUI

C5556684;

Disease excludes abnormal cell
- Malignant Squamous Cell [NCIt concept]
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease may have findings
- Globular Hyaline Body [NCIt concept]
Has associated anatomic sites
- Cervix Uteri [NCIt concept]
- Female Reproductive System [NCIt concept]
- Genitourinary System [NCIt concept]
- Reproductive System [NCIt concept]
- Uterus [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]
- Malignant Cuboidal Mucous Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Malignant Goblet-Like Mucous Cell [NCIt concept]
- Malignant Squamoid Cell [NCIt concept]
- Mucin-Producing Malignant Epithelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
disease_has_finding
- Carcinomatous Component Present [NCIt concept]
- Cystic Change [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Fibrotic Stroma Formation [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Cervix Epithelium [NCIt concept]
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Cervix Uteri [NCIt concept]
- Female Reproductive System [NCIt concept]
- Genitourinary System [NCIt concept]
- Uterus [NCIt concept]
disease_mapped_to_gene
- CRTC1/MAML2 Fusion Gene [NCIt concept]
- FHIT Gene [NCIt concept]
- MYC Gene [NCIt concept]
- TP53 Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(11;19)(q21;p13) [NCIt concept]
disease_may_have_molecular_abnormality
- CRTC1-MAML2 Fusion Protein Expression [NCIt concept]
- ERBB2 Gene Amplification [NCIt concept]
- FHIT Gene Inactivation [NCIt concept]
- MYC Gene Amplification [NCIt concept]
- TP53 Gene Inactivation [NCIt concept]

Keyword's position in hierarchy(ies) :

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