Gene table: search width pubmed_id = 30010796


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Mitochondrial myopathy, episodic with or withour atrophy and reversible leukoencephalopathy - (AR)
16.80
30010796
FDX2 (19p13.2)
Ferredoxin(M)
* Mitochondrial myopathy, episodic with or withour atrophy and reversible leukoencephalopathy - MEOAL