ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Lafora disease

Fatal multiple mitochondrial dysfunction syndrome

EPM2A	(UniProt - OMIM)		BOLA3	(UniProt - OMIM)
NHLRC1	(UniProt - OMIM)		NFU1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EPM2A	(0.79)	NFU1

Citations in the biomedical literature:

Lafora disease		Fatal multiple mitochondrial dysfunction syndrome
	Synonym(s): - Progressive myoclonic epilepsy type 2		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: D020192		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.