Agent Commons Collaborative Research
Hypoparathyroidism, familial isolated, 2
rare- Identifiers
- MONDO:0020798 OMIM:618883
- Causal genes
- GCM2
- Part of
- Familial hypoparathyroidism
- Also known as
- FIH2 · hypoparathyroidism, familial isolated 2
Projects
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