Benign neoplasm of parathyroid gland

Summary

Benign neoplasm of parathyroid gland (MONDO:0021463) is a cancer. A subtype of benign endocrine neoplasm — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	benign neoplasm of parathyroid gland
Mondo ID	MONDO:0021463
DOID	DOID:60008
ICD-10-CM	D35.1
ICD-11	455097662
NCIT	C3630
SNOMED CT	92272009
UMLS	C0154041
MedGen	57814
Anatomy (UBERON)	UBERON:0001132
Is cancer (heuristic)	yes

Also known as: benign neoplasm of parathyroid · benign neoplasm of the parathyroid · benign neoplasm of the parathyroid gland · benign parathyroid gland neoplasm · benign parathyroid gland tumor · benign parathyroid gland tumour · benign parathyroid neoplasm · benign parathyroid tumor · benign parathyroid tumour · benign tumor of parathyroid · benign tumor of parathyroid gland · benign tumor of the parathyroid · benign tumor of the parathyroid gland · benign tumour of parathyroid · benign tumour of parathyroid gland · benign tumour of the parathyroid · benign tumour of the parathyroid gland · parathyroid gland benign neoplasm · parathyroid tumor benign · parathyroid tumour benign

Data availability: 2 cell lines.

Disease family

This is a subtype of benign endocrine neoplasm. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › endocrine gland neoplasm › benign endocrine neoplasm › benign neoplasm of parathyroid gland

Related subtypes (13): liver lipoma, liver hemangioma, bile duct papillary neoplasm, liver leiomyoma, benign carotid body paraganglioma, benign thyroid gland neoplasm, pineocytoma, hepatocellular adenoma, benign neoplasm of pituitary gland, benign neoplasm of adrenal gland, benign neoplasm of thymus, TMEM127-related tumor predisposition, MAX-related tumor predisposition

Subtypes (1): parathyroid gland adenoma

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.