Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 3.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Meier-Gorlin syndrome 6, OMIM:616835, Meier-Gorlin syndrome 6, MONDO:0014794 |
Green in Severe microcephalyR-numbers: R88 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes MPD, microcephalic primordial dwarfism, Meier-Gorlin syndrome 6, 616835, MGORS6, primordial dwarfism |