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

RLBP1 PRPH2
RDH5
RHO
RLBP1


COMMON
GENES
RLBP1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
RLBP1
(0.85)
RDH5



Citations in the biomedical literature:


Bothnia retinal dystrophy
RLBP1
Retinitis punctata albescens
PRPH2 RDH5 RHO



Bothnia retinal dystrophy
Retinitis punctata albescens

Synonym(s):
- Västerbotten dystrophy

Synonym(s):
(no synonyms)

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:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.