ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 associated genes
7 signs/symptoms

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Mantle cell lymphoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RRM2B	(0.72)	ATM

Citations in the biomedical literature:

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy		Mantle cell lymphoma
	Synonym(s): - Adult-onset CPEO with mitochondrial myopathy		Synonym(s): - LCM - MCL - Mantle zone lymphoma

	Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: adult Type of inheritance: multigenic/multifactorial

	External references: No OMIM references No MeSH references		External references: No OMIM references 1 MeSH reference: D020522

Mantle cell lymphoma
	Very frequent - Hematologic / blood / lymphatic cancer - Lymphadenopathy / polyadenopathies Frequent - Anorexia - Asthenia / fatigue / weakness - Bone marrow / medullar infiltration - Splenomegaly - Weight loss / loss of appetite / break in weight curve / general health alteration
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
(no data available)