711152006: Autosomal dominant hypocalcemia (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

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

Expanded Value Set

This concept is not in any reference sets

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