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MRCS syndrome
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
Retinitis pigmentosa
Retinopathy, Burgess-Black type
Synonym(s):
- Microcornea - rod-cone dystrophy - cataract - posterior staphyloma
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
BEST1 O76090607854
No signs/symptoms info available.