25010000: Benign adult cystinosis (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Cystinosis\Benign adult cystinosis
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystinosis\Benign adult cystinosis
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Cystinosis\Benign adult cystinosis
• \Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Amino acid transport disorder\Cystinosis\Benign adult cystinosis
• \Metabolic disease\Metabolic disorder of transport\Amino acid transport disorder\Cystinosis\Benign adult cystinosis
• \Congenital disease\Inborn error of metabolism\Storage disease\Cystinosis\Benign adult cystinosis

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1224326011	Benign adult nephropathic cystinosis	en	Synonym	Active	Case insensitive	SNOMED CT core
41913018	Benign adult cystinosis	en	Synonym	Active	Case insensitive	SNOMED CT core
41914012	Benign cystinosis	en	Synonym	Active	Case insensitive	SNOMED CT core
754712019	Benign adult cystinosis (disorder)	en	Fully specified name	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

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