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Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant progressive external ophthalmoplegia
5 OMIM references -
5 associated genes
No signs/symptoms info
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Autosomal dominant progressive external ophthalmoplegia

RRM2B
(UniProt - OMIM)
 C10ORF2
(UniProt - OMIM)
POLG
(UniProt - OMIM)
POLG2
(UniProt - OMIM)
RRM2B
(UniProt - OMIM)
SLC25A4
(UniProt - OMIM)

COMMON
GENES 		RRM2B


Citations in the biomedical literature:


Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
RRM2B
Autosomal dominant progressive external ophthalmoplegia
C10ORF2 POLG POLG2 SLC25A4



Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Autosomal dominant progressive external ophthalmoplegia

Synonym(s):
- Adult-onset CPEO with mitochondrial myopathy
Synonym(s):
- adPEO
Classification (Orphanet):
- Inborn errors of metabolism
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
5 OMIM references -
No MeSH references
No signs/symptoms info available.