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, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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