ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Lafora disease

Early-onset Lafora body disease

EPM2A	(UniProt - OMIM)		PRDM8	(UniProt)
NHLRC1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NHLRC1	(0.63)	PRDM8

Citations in the biomedical literature:

Lafora disease		Early-onset Lafora body disease
	Synonym(s): - Progressive myoclonic epilepsy type 2		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

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

	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: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.