Gene table: search width pubmed_id = 27438479


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

protein
All allelic disease phenotypes - locus/disease symbols
Mitochondrial complex I deficiency due to ACAD9 deficiency - (AR)
9.25
27438479
ACAD9 (3q21.3)
Acyl-CoA dehydrogenase family member 9(M)
* Mitochondrial complex 1 deficiency, nuclear type 20 - MC1DN20