Disease

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

疾病靶点研报
Multiple Mitochondrial Dysfunctions Syndrome Type 1

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