TMEM70-related mitochondrial encephalo-cardio-myopathy

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Name:
TMEM70-related mitochondrial encephalo-cardio-myopathy
Description:
Mitochondrial encephalo-cardio-myopathy due to TMEM70 mutation is characterized by early neonatal onset of hypotonia, hypetrophic cardiomyopathy and apneic spells within hours after birth accompanied by lactic acidosis, hyperammonemia and 3-methylglutaconic aciduria.
ORPHAcode:
1194
Synonyms:
Mitochondrial encephalo-cardio-myopathy due to F1Fo ATPase deficiency
Mitochondrial encephalo-cardio-myopathy due to isolated ATP synthase deficiency
Mitochondrial encephalo-cardio-myopathy due to isolated mitochondrial respiratory chain complex V deficiency
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14