| Term Name: | autosomal dominant hypocalcemia 2 |
|---|---|
| Synonyms: | HYPOC2 |
| Definition: | An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13. |
| Ontology: | Human Disease [DOID:0090108] ( DOID:0090108 ) |