Any mitochondrial DNA depletion syndrome in which the cause of the disease is a mutation in the DGUOK gene.
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severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
MONDO:0007064
adenylosuccinate lyase deficiency
MONDO:0007068
familial juvenile hyperuricemic nephropathy type 1
MONDO:0008073
mitochondrial DNA depletion syndrome 4a
MONDO:0008758
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
MONDO:0009747
mitochondrial DNA depletion syndrome 7 (hepatocerebral type)
MONDO:0010060