Recurrent Lip Basal Cell Carcinoma

Preferred Label : Recurrent Lip Basal Cell Carcinoma;

NCIt synonyms : Recurrent Basal Cell Carcinoma of the Lip; Recurrent Basal Cell Carcinoma of Lip; Relapsed Lip Basal Cell Carcinoma; Relapsed Basal Cell Carcinoma of the Lip; Relapsed Basal Cell Carcinoma of Lip;

NCIt related terms : Recurrent Lip Basal Cell Cancer;

NCIt definition : Reemergence of basal cell carcinoma of the lip after a period of remission.;

Neoplastic status : Malignant;

Détails

Origin ID

C8213;

UMLS CUI

C0280364;

Disease excludes abnormal cell
- Malignant Stromal Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Excludes anatomical site(s)
- Hair Follicle [NCIt concept]
Has associated anatomic sites
- Head and Neck [NCIt concept]
- Integumentary System [NCIt concept]
- Lip [NCIt concept]
- Lip and Oral Cavity [NCIt concept]
- Skin [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Malignant Basal Cell [NCIt concept]
- Malignant Cell [NCIt concept]
- Malignant Cutaneous Basal Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Basaloid Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
disease_has_finding
- Carcinomatous Component Present [NCIt concept]
- Cutaneous Involvement [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Recurrent Disease [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Skin Basal Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Head and Neck [NCIt concept]
- Lip [NCIt concept]
- Lip and Oral Cavity [NCIt concept]
- Skin [NCIt concept]
disease_mapped_to_gene
- PTCH1 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- Inactivating PTCH1 Gene Mutation [NCIt concept]

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