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| Term | autosomal dominant hypocalcemia 1 | ID (Ontology) | DOID:0090107 (Human Disease) |
| Definition | An autosomal dominant hypocalcemia disease that has_material_basis_in heterozygous mutation in the calcium sensing receptor gene (CASR) on chromosome 3q21. | ||
| Also Known As | "HYPOC1" | ||
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autosomal dominant disease__ metal metabolism disorder___| autosomal dominant hypocalcemia |__autosomal dominant hypocalcemia 1 |
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| Is a | autosomal dominant hypocalcemia | ||
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| MIM:601198 | |||