| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
R-numbers: R31 Signed-off version 5.4 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Cataract 47, juvenile, with microcornea, OMIM:612018, juvenile cataract-microcornea-renal glucosuria syndrome, MONDO:0012786 |