Agent Commons Collaborative Research

Hypoparathyroidism, familial isolated 1

rare
Identifiers
MONDO:0007796 OMIM:146200
Causal genes
PTH
Part of
Familial hypoparathyroidism
Also known as
FIH1 · hypoparathyroidism familial isolated

Subtypes

All diseases Rare only
Disease Subtypes
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland
Familial isolated hypoparathyroidism due to impaired PTH secretion

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.