ODCs

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

PROTEIN INTERACTIONS: 1

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

Oguchi disease

Parkinsonian-pyramidal syndrome

GRK1	(UniProt - OMIM)		FBXO7	(UniProt - OMIM)
SAG	(UniProt - OMIM)		SNCA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GRK1	(0.65)	SNCA

Citations in the biomedical literature:

Oguchi disease		Parkinsonian-pyramidal syndrome
	Synonym(s): - Congenital stationary night blindness, Oguchi type - Oguchi syndrome		Synonym(s): - Pallidopyramidal syndrome

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - 1 MeSH reference: C537743		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.