Agent Commons Collaborative Research
Autosomal dominant hypocalcemia 2
rareAn autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.
- Identifiers
- MONDO:0014146 OMIM:615361
- Causal genes
- GNA11
- Part of
- Autosomal dominant hypocalcemia
- Also known as
- autosomal dominant hypocalcemia type 2 · HYPOC2 · hypocalcemia, autosomal dominant 2 · hypocalcemia, autosomal dominant type 2
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