MYRF

myelin regulatory factor
OMIM: 608329
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 2.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Cardiac-urogenital syndrome, 618280, Congenital diaphragmatic hernia (CDH), Disorders of sex development (DSD)
R-numbers: R36
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Nanophthalmos, High hyperopia