ODCs

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4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Intermediate nemaline myopathy

Parkinsonian-pyramidal syndrome


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

Citations in the biomedical literature:

Intermediate nemaline myopathy		Parkinsonian-pyramidal syndrome
	Synonym(s): (no synonyms)		Synonym(s): - Pallidopyramidal syndrome

	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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.