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Myopathy with Lactic Acidosis, Hereditary MeSH Supplementary Concept Data 2023


MeSH Supplementary
Myopathy with Lactic Acidosis, Hereditary
Unique ID
C564972
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564972
Entry Term(s)
Hereditary Myopathy with Lactic Acidosis
Iron-Sulfur Cluster Deficiency Myopathy
Myoglobinuria due to Abnormal Glycolysis
Myopathy with Deficiency of ISCU
Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme
Myopathy with Deficiency of Succinate Dehydrogenase and Aconitase
Myopathy with Exercise Intolerance, Swedish Type
Registry Number
0
Heading Mapped to
Acidosis, Lactic / *congenital
Muscular Diseases / *congenital
Frequency
5
Date of Entry
2012/11/05
Revision Date
2013/10/24
Myopathy with Lactic Acidosis, Hereditary Preferred
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