ODCs

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

PROTEIN INTERACTIONS: 2

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

Parkinsonian-pyramidal syndrome

Genetic recurrent myoglobinuria


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SNCA SNCA	(0.73) (0.49)	MT-CO3 MT-CO1

Citations in the biomedical literature:

Parkinsonian-pyramidal syndrome		Genetic recurrent myoglobinuria
	Synonym(s): - Pallidopyramidal syndrome		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -

	Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.