Childhood Pilomatricoma

Preferred Label : Childhood Pilomatricoma;

NCIt synonyms : Pediatric Pilomatricoma;

NCIt definition : A pilomatricoma that occurs during childhood.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL1799015;

Détails

Origin ID

C190279;

UMLS CUI

C5783606;

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
- Calcification [NCIt concept]
Has associated anatomic sites
- Adnexa [NCIt concept]
- Integumentary System [NCIt concept]
- Skin [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
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]
disease_has_finding
- Adnexal Differentiation [NCIt concept]
- Benign Cellular Infiltrate [NCIt concept]
- Childhood Lesion [NCIt concept]
- Cutaneous Involvement [NCIt concept]
- Cystic Change [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Follicular Differentiation [NCIt concept]
- Shadow Cells Present [NCIt concept]
- Skin Nodule [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Exocrine System [NCIt concept]
- Hair [NCIt concept]
- Hair Follicle [NCIt concept]
- Skin [NCIt concept]
- Skin Adnexa [NCIt concept]
disease_mapped_to_gene
- CTNNB1 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- CTNNB1 Gene Mutation [NCIt concept]

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