| Panel | Mode of inheritance | Details |
|---|---|---|
2 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 7.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Oculovertebral syndrome, OMIM:621277 |
Green in Structural eye diseaseR-numbers: R36 Signed-off version 5.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes coloboma, MONDO:0001476, microphthalmia, MONDO:0021129, Oculovertebral syndrome, OMIM:621277, oculovertebral syndrome, MONDO:0979866 |