Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
R-numbers: R101 Signed-off version 3.21 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Cutis laxa, autosomal recessive, type ID, OMIM:620780, cutis laxa, MONDO:0016175 |
Green in Retinal disordersR-numbers: R32 Signed-off version 7.8 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Doyne honeycomb degeneration of retina, OMIM:126600 |