C21orf59

chromosome 21 open reading frame 59
OMIM: 615494
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliary dyskinesia, primary, 26, OMIM:615500, Primary ciliary dyskinesia 26, MONDO:0014211
R-numbers: R139
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliary dyskinesia, primary, 26, 615500
R-numbers: R189
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliary dyskinesia, primary, 26, 615500