Multiple Mitochondrial Dysfunctions Syndrome Type 1

About the Disease
Multiple Mitochondrial Dysfunctions Syndrome 1, also known as mmds1, is related to multiple mitochondrial dysfunctions syndrome 4 and pyruvate dehydrogenase e1-alpha deficiency, and has symptoms including lethargy and weakness. An important gene associated with Multiple Mitochondrial Dysfunctions Syndrome 1 is NFU1 (NFU1 Iron-Sulfur Cluster Scaffold), and among its related pathways/superpathways are Metabolism and Glyoxylate metabolism and glycine degradation. Affiliated tissues include brain, prostate and myeloid, and related phenotypes are failure to thrive and hypertension

Common Targets
NFU1

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