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Retinal macular dystrophy type 2
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Cone rod dystrophy
Retinitis pigmentosa
Stargardt disease
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Synonym(s):
- MCDR2
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
PROM1 O43490604365
No signs/symptoms info available.