| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Retinal disordersR-numbers: R32 Signed-off version 9.0 | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Phenotypes Retinitis pigmentosa 99, OMIM:301148, retinitis pigmentosa 99, MONDO:0978291 |