NME5

NME/NM23 family member 5
OMIM: 603575
PanelMode of inheritanceDetails
1 panel
R-numbers: R189
Signed-off version 3.25
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliary dyskinesia, primary, 48, without situs inversus, OMIM:620032