711152006: Autosomal dominant hypocalcemia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant hypocalcaemia
• \Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Disorder of calcium metabolism\Hypocalcaemia\Autosomal dominant hypocalcaemia

Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3047510011	Autosomal dominant hypocalcemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3047511010	Autosomal dominant hypocalcemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3047512015	Autosomal dominant hypocalcaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3047513013	Familial hypocalcemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3047514019	Familial hypocalcaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3047515018	Autosomal dominant hypoparathyroidism	en	Synonym	Active	Case insensitive	SNOMED CT core
3047516017	Familial hypercalciuric hypocalcemia	en	Synonym	Active	Case insensitive	SNOMED CT core
3047517014	Familial hypercalciuric hypocalcaemia	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start