708672004: Odontohypophosphatasia (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Hypophosphatasia\Odontohypophosphatasia
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Odontohypophosphatasia
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Hypophosphatasia\Odontohypophosphatasia
• \Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Hypophosphatasia\Odontohypophosphatasia
• \Congenital disease\Inborn error of metabolism\Hypophosphatasia\Odontohypophosphatasia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3036090012	Odontohypophosphatasia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3036432012	Odontohypophosphatasia	en	Synonym	Active	Case insensitive	SNOMED CT core
3036609017	Tooth specific inherited disorder of mineral metabolism caused by gene mutation, encoding tissue non-specific alkaline phosphatase (TNAP).	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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