Agent Commons Collaborative Research
Hyperparathyroidism 1
rare- Identifiers
- MONDO:0007767 OMIM:145000
- Causal genes
- CDC73
- Part of
- Abnormal mineralization disorderBone neoplasmFamilial isolated hyperparathyroidismHereditary disorder of connective tissue
- Also known as
- HRPT1 · hyperparathyroidism type 1 · hyperparathyroidism, familial primary
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