Familial primary hyperparathyroidism

rare

An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome.

Identifiers: MONDO:0016365 Orphanet:2207
Part of: Hereditary hyperparathyroidism Primary hyperparathyroidism Tumor of parathyroid gland
Also known as: hereditary primary hyperparathyroidism (disease)

Subtypes

Disease	ID	Subtypes	Genes
Familial isolated hyperparathyroidism	MONDO:0015027	3
Hyperparathyroidism 2 with jaw tumors	MONDO:0007768
Hyperparathyroidism, primary, caused by water clear cell hyperplasia	MONDO:0044350
Multiple endocrine neoplasia type 1	MONDO:0007540		MEN1
Neonatal severe primary hyperparathyroidism	MONDO:0009397		CASR

Rare disease

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