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1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
2 OMIM references -
2 associated genes
No signs/symptoms info
Retinitis punctata albescens
Oguchi disease

PRPH2 GRK1
RDH5 SAG
RHO
RLBP1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
RHO
RHO
(0.83)
(0.8)
SAG
GRK1



Citations in the biomedical literature:


Retinitis punctata albescens
PRPH2 RDH5 RHO RLBP1
Oguchi disease
GRK1 SAG



Retinitis punctata albescens
Oguchi disease

Synonym(s):
(no synonyms)

Synonym(s):
- Congenital stationary night blindness, Oguchi type
- Oguchi syndrome

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

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

Epidemiological data:
Class of prevalence: -
Average age onset: childhood
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:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C537743

No signs/symptoms info available.