MeSH Browser

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 Numbers: 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 MeSH Supplementary Concept Data 2025