ODCs

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

PROTEIN INTERACTIONS: 1

4 associated genes
No signs/symptoms info

Parkinsonian-pyramidal syndrome

Intermediate nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SNCA	(0.56)	ACTA1

Citations in the biomedical literature:

Parkinsonian-pyramidal syndrome		Intermediate nemaline myopathy
	Synonym(s): - Pallidopyramidal syndrome		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: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

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

No signs/symptoms info available.