RS104893632 DGUOK
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
Inborn genetic diseases
DGUOK-related disorder
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 4
Portal hypertension
noncirrhotic
1
Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
Inborn genetic diseases
DGUOK-related disorder
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 4
Portal hypertension
noncirrhotic
Other Variants in DGUOK