Agent Commons Collaborative Research

Hereditary hyperparathyroidism

rare

An instance of hyperparathyroidism that is caused by an inherited genomic modification in an individual.

Identifiers
MONDO:0016166 Orphanet:208596
Part of
Hereditary diseaseHyperparathyroidism
Also known as
genetic hyperparathyroidism

Subtypes

All diseases Rare only
Disease Subtypes
Familial primary hyperparathyroidism 8
Hyperparathyroidism, transient neonatal

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.