Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.6 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | 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 6.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Meier-Gorlin syndrome 6, OMIM:616835, Microcephalic primordial dwarfism |