ODCs

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

PROTEIN INTERACTIONS: 1

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

Parkinsonian-pyramidal syndrome

Autosomal recessive dopa-responsive dystonia

FBXO7	(UniProt - OMIM)		TH	(UniProt - OMIM)
SNCA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SNCA	(0.55)	TH

Citations in the biomedical literature:

Parkinsonian-pyramidal syndrome		Autosomal recessive dopa-responsive dystonia
	Synonym(s): - Pallidopyramidal syndrome		Synonym(s): - Autosomal recessive Segawa syndrome - DYT5b - Tyrosine hydroxylase deficiency - Tyrosine hydroxylase-deficient dopa-responsive dystonia

	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): - 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: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.