1187515001: Mitochondrial phosphate carrier deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Mitochondrial phosphate carrier deficiency
• \Metabolic disease\Mitochondrial cytopathy\Mitochondrial metabolism defect\Mitochondrial phosphate carrier deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4674059019	Mitochondrial phosphate carrier deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4674060012	Mitochondrial phosphate carrier deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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