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Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency MeSH Supplementary Concept Data 2023


MeSH Supplementary
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
Unique ID
C567528
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567528
Registry Number
0
Heading Mapped to
*Mitochondrial Encephalomyopathies
Mitochondrial Proton-Translocating ATPases / *deficiency
Frequency
1
Note
mutations in TMEM70
Date of Entry
2012/11/05
Revision Date
2013/11/06
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Preferred
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