ODCs

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

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Leigh syndrome with nephrotic syndrome

Multiple system atrophy, parkinsonian type

Citations in the biomedical literature:

Leigh syndrome with nephrotic syndrome		Multiple system atrophy, parkinsonian type
	Synonym(s): - Infantile subacute necrotizing encephalopathy with nephrotic syndrome - Leigh disease with nephrotic syndrome		Synonym(s): - MSA, parkinsonian type - MSA-p

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

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

	Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.