GMNN

geminin, DNA replication inhibitor
OMIM: 602842
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Meier-Gorlin syndrome 6, OMIM:616835, Meier-Gorlin syndrome 6, MONDO:0014794
R-numbers: R88
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
MPD, microcephalic primordial dwarfism, Meier-Gorlin syndrome 6, 616835, MGORS6, primordial dwarfism