NEK9

NIMA related kinase 9
OMIM: 609798
PanelMode of inheritanceDetails
2 panels
R-numbers: R83
Signed-off version 4.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Arthrogryposis, Perthes disease, and upward gaze palsy, OMIM:614262, Arthrogryposis, Perthes disease, and upward gaze palsy, MONDO:0013660, Lethal congenital contracture syndrome 10, OMIM:617022, NEK9-related lethal skeletal dysplasia, MONDO:0014870
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Arthrogryposis, Perthes disease, and upward gaze palsy, OMIM:614262, Arthrogryposis, Perthes disease, and upward gaze palsy, MONDO:0013660, Lethal congenital contracture syndrome 10, OMIM:617022, NEK9-related lethal skeletal dysplasia, MONDO:0014870