Parathyroid Gland Adenoma

Preferred Label : Parathyroid Gland Adenoma;

NCIt related terms : ADENOMA, PARATHYROID GLAND, BENIGN;

NCIt definition : A benign ovoid parathyroid gland neoplasm surrounded by a pseudocapsule. It is composed of chief cells, clear cells, oncocytic cells, or a mixture of cell types. It lacks the morphological characteristics of parathyroid gland carcinoma and there is no evidence of capsular invasion, vascular invasion, and perineural invasion.;

Alternative definition : CDISC: A benign neoplasm arising from the Chief cells of the parathyroid gland.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL935888;

Details

Origin ID

C156757;

UMLS CUI

C0262587;

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 adenoma [MedDRA LLT]
- Parathyroid adenoma [HPO term]
- Parathyroid adenoma (disorder) [SNOMED CT concept]
- parathyroid adenoma [MeSH concept]
- parathyroid adenoma [DO Concept]
- parathyroid adenoma [Disease (Nov.)]
Validated automatic mappings to NTBT
- parathyroid adenoma [DO Concept]
concept_is_in_subset
- CDISC SEND Terminology [NCIt concept]
- CDISC SEND Tumor Findings Results Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- Clinical Data Interchange Standards Consortium 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 Parathyroid Gland 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]
may_be_associated_disease_of_disease
- Hyperparathyroidism-Jaw Tumor Syndrome [NCIt concept]
- Multiple Endocrine Neoplasia Type 1 [NCIt concept]
- Multiple Endocrine Neoplasia Type 4 [NCIt concept]
- Multiple Endocrine Neoplasia Type 5 [NCIt concept]
pathogenesis_of_disease_involves_gene
- CCND1 Gene [NCIt concept]
- CCND1 wt Allele [NCIt concept]
- MEN1 Gene [NCIt concept]
- MEN1 wt Allele [NCIt concept]

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