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Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
MeSH Supplementary Concept Data 2023
Details
Concepts
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
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Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
Preferred
Concept UI
M0567828
Registry Number
0
Terms
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency
Preferred Term
Term UI
T810612
Date
11/15/2011
LexicalTag
NON
ThesaurusID
OMIM (2013)
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