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Early-onset Lafora body disease
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Lafora disease
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
PRDM8 Q9NQV8
No signs/symptoms info available.