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Unverricht-Lundborg disease
3 OMIM references -
3 associated genes
No signs/symptoms info
COMMON GENES: 1
Action myoclonus - renal failure syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Unverricht-Lundborg disease
Action myoclonus - renal failure syndrome

CSTB
(UniProt - OMIM)
 SCARB2
(UniProt - OMIM)
PRICKLE1
(UniProt - OMIM)
SCARB2
(UniProt - OMIM)

COMMON
GENES 		SCARB2


Citations in the biomedical literature:


Unverricht-Lundborg disease
CSTB PRICKLE1 SCARB2
Action myoclonus - renal failure syndrome



Unverricht-Lundborg disease
Action myoclonus - renal failure syndrome

Synonym(s):
- Progressive myoclonic epilepsy type 1
- ULD
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal 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:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
External references:
3 OMIM references -
1 MeSH reference: D020194
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.