# autosomal dominant hypocalcemia 2

> autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13

**Wikidata**: [Q30989619](https://www.wikidata.org/wiki/Q30989619)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-hypocalcemia-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)