MRCS syndrome https://www.malacards.org/card/mrcs_syndrome MONDO:0016979 UMLS:C4749856 MRCS syndrome is a rare, genetic retinal dystrophy disorder characterized by bilateral microcornea, rod-cone dystrophy, cataracts and posterior staphyloma, in the absence of other systemic features. Night blindness is typically the presenting manifestation and nystagmus, strabismus, astigmatism and angle closure glaucoma may be associated findings. Progressive visual acuity deterioration, due to pulverulent-like cataracts, results in poor vision ranging from no light perception to 20/400. microcornea-rod-cone dystrophy-cataract-posterior staphyloma syndrome GARD:0017255 MEDGEN:1666962 icd11.foundation:392681472 Orphanet:263347 inherited retinal dystrophy