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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

DGUOK DGUOK


COMMON
GENES
DGUOK



Citations in the biomedical literature:


Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
DGUOK
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency



Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- Adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.