Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in Structural eye diseaseR-numbers: R36 Signed-off version 3.79 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Singleton-Merten syndrome 2, OMIM:616298, Singleton-Merten syndrome 2, MONDO:0014575 |