Low Grade Esophageal Squamous Intraepithelial Neoplasia

Preferred Label : Low Grade Esophageal Squamous Intraepithelial Neoplasia;

NCIt synonyms : Esophageal Low Grade Squamous Intraepithelial Neoplasia; Low Grade Esophageal Squamous Dysplasia; Esophageal Low-Grade Squamous Intraepithelial Neoplasia;

NCIt related terms : Esophageal squamous intraepithelial neoplasia (dysplasia), low grade;

NCIt definition : A lesion in which the architectural and cytologic abnormalities are confined to the lower half of the esophageal squamous epithelium.;

Neoplastic status : Undetermined;

ICD-O code : 8077/0;

Détails

Origin ID

C27427;

UMLS CUI

C1333458;

Automatic exact mappings (from CISMeF team)
- Oesophageal squamous intraepithelial neoplasia (dysplasia), low grade [ICD-11 Extension code]
Disease excludes abnormal cell
- Neoplastic Glandular Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Esophagus [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
disease_excludes_finding
- Invasive Lesion [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
disease_has_abnormal_cell
- Dysplastic Epithelial Cell [NCIt concept]
- Dysplastic Squamous Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
disease_has_finding
- Dysplasia [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Low Grade Lesion [NCIt concept]
- Mild Dysplasia [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Squamous Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Esophageal Mucosa [NCIt concept]
- Esophageal Squamous Epithelium [NCIt concept]
- Squamous Epithelium [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Esophagus [NCIt concept]
disease_may_have_molecular_abnormality
- CCND1 Gene Amplification [NCIt concept]
- Inactivating FHIT Gene Mutation [NCIt concept]
- TP53 Gene Inactivation [NCIt concept]

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

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