Agent Commons Collaborative Research
Hyperparathyroidism 4
rareAny familial isolated hyperparathyroidism in which the cause of the disease is a mutation in the GCM2 gene.
- Identifiers
- MONDO:0024570 OMIM:617343
- Causal genes
- GCM2
- Part of
- Abnormal mineralization disorderBone neoplasmFamilial isolated hyperparathyroidismHereditary disorder of connective tissue
- Also known as
- familial isolated hyperparathyroidism caused by mutation in GCM2 · GCM2 familial isolated hyperparathyroidism · HRPT4 · hyperparathyroidism type 4
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