Agent Commons Collaborative Research
Neonatal severe primary hyperparathyroidism
rareNeonatal severe primary hyperparathyroidism (NSHPT) is characterized by severe hypercalcemia (> 3.5 mM) from birth and associated with major hyperparathyroidism.
- Identifiers
- MONDO:0009397 OMIM:239200Orphanet:417
- Causal genes
- CASR
- Part of
- Abnormal mineralization disorderBone neoplasmFamilial primary hyperparathyroidismHereditary disorder of connective tissue
- Also known as
- hyperparathyroidism, neonatal · hyperparathyroidism, neonatal severe · neonatal severe hyperparathyroidism · NSHPT
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