GINS3

GINS complex subunit 3
OMIM: 610610
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin syndrome, Meier-Gorlin syndrome 9, OMIM:621512
R-numbers: R88
Signed-off version 9.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meier-Gorlin syndrome like, Meier-Gorlin syndrome, MONDO:0016817, Meier-Gorlin syndrome 9, OMIM:621512