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Bietti crystalline dystrophy
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Retinitis pigmentosa
Synonym(s):
- BCD
- Bietti crystalline corneoretinal dystrophy
- Bietti crystalline retinopathy
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CYP4V2 Q6ZWL3608614
No signs/symptoms info available.