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Retinopathy, Burgess-Black type
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Adult-onset foveomacular vitelliform dystrophy
Autosomal dominant vitreoretinochoroidopathy
Best vitelliform macular dystrophy
MRCS syndrome
Retinitis pigmentosa
Synonym(s):
- Autosomal recessive bestrophinopathy
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
BEST1 O76090607854
No signs/symptoms info available.