NOP10

NOP10 ribonucleoprotein
OMIM: 606471
PanelMode of inheritanceDetails
2 panels
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Class: BM failure syndrome (typ AR), Dyskeratosis congenita, MDS, AML, Oral and GI squamous cell carcinoma
R-numbers: R421
Signed-off version 1.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dyskeratosis congenita, autosomal recessive 1, OMIM:224230