Conventional Lipoma

Preferred Label : Conventional Lipoma;

NCIt synonyms : Classic Type Lipoma;

NCIt definition : A benign well-circumscribed tumor, composed of lobules of mature adipocytes, that arises within subcutaneous tissue, deep soft tissues or on the surface of bones.;

Neoplastic status : Benign;

Details

Origin ID

C27530;

UMLS CUI

C1333059;

Automatic exact mappings (from CISMeF team)
- conventional lipoma [DO Concept]
DO Cross reference
- conventional lipoma [DO Concept]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Neoplastic Lipoblast [NCIt concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Painless Mass [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- conventional lipoma [DO Concept]
disease_excludes_cytogenetic_abnormality
- Rearrangement of 8q11-q13 [NCIt concept]
disease_excludes_finding
- Locally Aggressive Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_excludes_molecular_abnormality
- PLAG1 Protein Overexpression [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Lipocyte [NCIt concept]
- Neoplastic Mature Adipocyte [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Localized Disease [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
disease_has_normal_cell_origin
- Adipocyte [NCIt concept]
- Connective and Soft Tissue Cell [NCIt concept]
disease_has_normal_tissue_origin
- Adipose Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Connective and Soft Tissue [NCIt concept]
disease_mapped_to_chromosome
- Human Chromosome 13 [NCIt concept]
disease_mapped_to_gene
- HMGA2 Gene [NCIt concept]
- HMGA2/LPP Long Fusion Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Loss of Chromosome 13q [NCIt concept]
- t(1;12)(p32-34;q13-15) [NCIt concept]
- t(2;12)(p22-24;q13-15) [NCIt concept]
- t(2;12)(q35-37;q13-15) [NCIt concept]
- t(5;12)(q33;q13-15) [NCIt concept]
pathogenesis_of_disease_involves_gene
- HMGA2 Gene [NCIt concept]
- HMGA2 wt Allele [NCIt concept]
- HMGA2/LPP Long Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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