1217212009: Mitochondrial pyruvate carrier deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\...
• \Disorder of pyruvate metabolism and mitochondrial respiratory chain\Inborn error of pyruvate metabolism\Mitochondrial pyruvate carrier deficiency
• \Inherited metabolic disorder of nervous system\Mitochondrial pyruvate carrier deficiency
• \Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Mitochondrial pyruvate carrier deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Mitochondrial pyruvate carrier deficiency
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Mitochondrial pyruvate carrier deficiency
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Mitochondrial pyruvate carrier deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\...
• \Disorder of pyruvate metabolism and mitochondrial respiratory chain\Inborn error of pyruvate metabolism\Mitochondrial pyruvate carrier deficiency
• \Inherited metabolic disorder of nervous system\Mitochondrial pyruvate carrier deficiency
• \Congenital disease\Inborn error of metabolism\...
• \Disorder of pyruvate metabolism and mitochondrial respiratory chain\Inborn error of pyruvate metabolism\Mitochondrial pyruvate carrier deficiency
• \Inherited metabolic disorder of nervous system\Mitochondrial pyruvate carrier deficiency

Status: current, Primitive. Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5035156010	Mitochondrial pyruvate carrier deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
5035157018	Mitochondrial pyruvate carrier deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5035158011	A rare pyruvate metabolism disorder with characteristics of neonatal onset of a mitochondrial encephalopathy with global developmental delay and the biochemical characteristics of lactic acidosis and increased serum pyruvate with normal lactate/pyruvate ratio. Additional reported manifestations include epilepsy, peripheral neuropathy, hypotonia, nystagmus, extensor plantar responses, hepatomegaly and craniofacial dysmorphism (such as progressive microcephaly, epicanthus, long philtrum, and thin upper lip).	en	Definition	Active	Case sensitive	SNOMED CT core

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