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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Dedifferentiated liposarcoma

RRM2B CDK4
HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
RRM2B
(0.77)
MDM2



Citations in the biomedical literature:


Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
RRM2B
Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2



Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Dedifferentiated liposarcoma

Synonym(s):
- mtDNA depletion syndrome, encephalomyopathic form with renal tubulopathy

Synonym(s):
- DDLS

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

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

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

No signs/symptoms info available.