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Parkinsonian-pyramidal syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Oguchi disease
2 OMIM references -
2 associated genes
No signs/symptoms info
Parkinsonian-pyramidal syndrome
Oguchi disease

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

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


Citations in the biomedical literature:


Parkinsonian-pyramidal syndrome
FBXO7 SNCA
Oguchi disease
GRK1 SAG



Parkinsonian-pyramidal syndrome
Oguchi disease

Synonym(s):
- Pallidopyramidal syndrome
Synonym(s):
- Congenital stationary night blindness, Oguchi type
- Oguchi syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the eye and adnexa -
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: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C537743
No signs/symptoms info available.