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Retinitis punctata albescens
1 OMIM reference -
4 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Bothnia retinal dystrophy
1 OMIM reference -
1 associated gene
No signs/symptoms info
Retinitis punctata albescens
Bothnia retinal dystrophy

PRPH2
(UniProt - OMIM)
 RLBP1
(UniProt - OMIM)
RDH5
(UniProt - OMIM)
RHO
(UniProt - OMIM)
RLBP1
(UniProt - OMIM)

COMMON
GENES 		RLBP1
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RDH5
(0.85)
RLBP1


Citations in the biomedical literature:


Retinitis punctata albescens
PRPH2 RDH5 RHO RLBP1
Bothnia retinal dystrophy



Retinitis punctata albescens
Bothnia retinal dystrophy

Synonym(s):
(no synonyms)

Synonym(s):
- Västerbotten dystrophy
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:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.