ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

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

Action myoclonus - renal failure syndrome

Unverricht-Lundborg disease

Citations in the biomedical literature:

Action myoclonus - renal failure syndrome		Unverricht-Lundborg disease
	Synonym(s): (no synonyms)		Synonym(s): - Progressive myoclonic epilepsy type 1 - ULD

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - 1 MeSH reference: D020194

No signs/symptoms info available.