has material basis in germline mutation in
RDH12
inherited retinal dystrophy
RDH12-related recessive retinopathy
https://github.com/monarch-initiative/mondo/issues/4937
RDH12 Leber congenital amaurosis
A retinopathy, typically severe, and early onset, caused by biallelic variants in the RDH12 gene.
retinitis pigmentosa 53
Leber congenital amaurosis type 13
Leber congenital amaurosis caused by mutation in RDH12
Leber congenital amaurosis 13
LCA13
MONDO:0800099
RDH12-related recessive retinopathy