NME5

NME/NM23 family member 5
OMIM: 603575, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber NME5 in Respiratory ciliopathies including non-CF bronchiectasis Version 3.10 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Ciliary dyskinesia, primary, 48, without situs inversus, OMIM:620032 Tags watchlist Q4_23_promote_green Q4_23_NHS_review

Panel

Reviews

Mode of inheritance

Details

Version 3.10
Latest signed off version: v3.0 (22 Mar 2023)

review

BIALLELIC, autosomal or pseudoautosomal