Parathyroid Gland Clear Cell Adenoma

Preferred Label : Parathyroid Gland Clear Cell Adenoma;

NCIt synonyms : Clear Cell Adenoma of the Parathyroid Gland; Transitional Clear Cell Adenoma of Parathyroid; Transitional Clear Cell Adenoma of Parathyroid Gland; Clear Cell Adenoma of the Parathyroid; Clear Cell Adenoma of Parathyroid; Parathyroid Transitional Clear Cell Adenoma; Clear Cell Adenoma of Parathyroid Gland; Parathyroid Clear Cell Adenoma; Parathyroid Gland Transitional Clear Cell Adenoma; Transitional Clear Cell Adenoma of the Parathyroid Gland; Transitional Clear Cell Adenoma of the Parathyroid;

NCIt definition : A parathyroid gland adenoma composed predominantly of neoplastic cells with clear cytoplasm.;

Neoplastic status : Benign;

Details

Origin ID

C7993;

UMLS CUI

C0279700;

Automatic exact mappings (from CISMeF team)
- parathyroid transitional clear cell adenoma [DO Concept]
Currated CISMeF NLP mapping
- Parathyroid transitional clear cell adenoma [MedDRA LLT]
DO Cross reference
- parathyroid transitional clear cell adenoma [DO Concept]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Endocrine 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
- Acinar Pattern [NCIt concept]
- Encapsulated Mass [NCIt concept]
- Follicular Structures Present [NCIt concept]
- Solid Growth Pattern [NCIt concept]
- Trabecular Pattern [NCIt concept]
Has associated anatomic sites
- Head and Neck [NCIt concept]
- Neck [NCIt concept]
- Parathyroid Gland [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Parathyroid transitional clear cell adenoma [MedDRA LLT]
- parathyroid transitional clear cell adenoma [DO Concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_excludes_cytogenetic_abnormality
- Loss of Chromosome 11q [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 16q [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
- Loss of Chromosome 9q [NCIt concept]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Broad Fibrous Bands Formation [NCIt concept]
- Capsular Invasion [NCIt concept]
- Hemosiderin Deposition [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mitotic Activity [NCIt concept]
- Perineural Invasion [NCIt concept]
- Tumor Vascular Invasion [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Endocrine Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Epithelial Clear Cell [NCIt concept]
- Neoplastic Parathyroid Gland Cell [NCIt concept]
- Neoplastic Parathyroid Gland Clear Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Endocrine Differentiation [NCIt concept]
- Epithelial Component Present [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Parathyroid Gland Parenchymal Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Parathyroid Gland Epithelial Tissue [NCIt concept]
- Parathyroid Gland Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Head and Neck [NCIt concept]
- Neck [NCIt concept]
- Parathyroid Gland [NCIt concept]
disease_mapped_to_gene
- CCND1 Gene [NCIt concept]
- MEN1 Gene [NCIt concept]
disease_may_have_associated_disease
- Primary Hyperparathyroidism [NCIt concept]
disease_may_have_molecular_abnormality
- Aneuploidy [NCIt concept]
- MEN1 Gene Inactivation [NCIt concept]

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