Eyelid Seborrheic Keratosis

Preferred Label : Eyelid Seborrheic Keratosis;

NCIt synonyms : Eyelid Basal Cell Papilloma; Seborrheic Keratosis of Eyelid; Basal Cell Papilloma of the Eyelid; Seborrheic Keratosis of the Eyelid; Basal Cell Papilloma of Eyelid;

NCIt definition : A benign skin neoplasm that arises from the eyelid. It is characterized by the intraepidermal proliferation of basaloid keratinocytes, acanthosis, hyperkeratosis, and cysts formation.;

Neoplastic status : Benign;

Details

Origin ID

C4356;

UMLS CUI

C0339109;

Automatic exact mappings (from CISMeF team)
- Eyelid seborrheic keratosis [MedDRA LLT]
- Eyelid seborrhoeic keratosis [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Seborrheic keratosis of eyelid (disorder) [SNOMED CT concept]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease excludes normal cell origin
- Endocrine-Stromal Cell [NCIt concept]
Disease may have findings
- Papular Lesion [NCIt concept]
Excludes anatomical site(s)
- Lymphatic System [NCIt concept]
Has associated anatomic sites
- Eye [NCIt concept]
- Eyelid [NCIt concept]
- Integumentary System [NCIt concept]
- Skin [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Eyelid seborrheic keratosis [MedDRA LLT]
- Eyelid seborrhoeic keratosis [MedDRA Preferred Term]
- Seborrheic keratosis of eyelid (disorder) [SNOMED CT concept]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Dysplasia [NCIt concept]
- Invasive Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Keratinocyte [NCIt concept]
disease_has_finding
- Acanthosis [NCIt concept]
- Benign Cellular Infiltrate [NCIt concept]
- Cutaneous Involvement [NCIt concept]
- Cystic Change [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Hyperkeratosis [NCIt concept]
disease_has_normal_cell_origin
- Basal Cell of the Squamous Epithelium [NCIt concept]
- Epithelial Cell [NCIt concept]
- Keratinocyte [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Eye [NCIt concept]
- Eyelid [NCIt concept]
- Skin [NCIt concept]
disease_may_have_molecular_abnormality
- AKT1 Gene Mutation [NCIt concept]
- EGFR Gene Mutation [NCIt concept]
- FGFR3 Gene Mutation [NCIt concept]
- HRAS Gene Mutation [NCIt concept]
- KRAS Gene Mutation [NCIt concept]
- PIK3CA Gene Mutation [NCIt concept]

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