GMNN

geminin, DNA replication inhibitor
OMIM: 602842
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome
R-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
R-numbers: R88
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Meier-Gorlin syndrome 6, OMIM:616835, Microcephalic primordial dwarfism