Human genes for autosomal dominant hypocalcemia 2
Autosomal dominant hypocalcemia 2 [DOID:0090108]
An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13.
Synonyms: autosomal dominant hypocalcemia 2, DOID:0090108, HYPOC2