FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal dominant hypocalcemia 2 ID (Ontology) DOID:0090108 (Human Disease)
Definition An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13.
Also Known As "HYPOC2"
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 Genes
 autosomal dominant hypocalcemia 2       1
 for disease ribbon | autosomal dominant hypocalcemia 2       1
 model of | autosomal dominant hypocalcemia 2       1
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autosomal dominant disease__
metal metabolism disorder___|
                            autosomal dominant hypocalcemia
                             |__autosomal dominant hypocalcemia 2  1 rec.
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Is a autosomal dominant hypocalcemia
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Synonyms
  • "HYPOC2" EXACT OMO:0003012
Secondary IDs
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MIM:615361