DNAH9

dynein axonemal heavy chain 9
OMIM: 603330, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels
Amber DNAH9 in Haematological malignancies cancer susceptibility


Level 2: Cancer susceptibility
Version 5.1
Latest signed off version: v5.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • MDS/AML
  • inherited bone marrow failure (IBMF)
Green DNAH9 in Primary ciliary disorders

Level 3: Respiratory ciliopathies
Level 2: Ciliopathies
Version 1.56

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 40, OMIM:618300
  • ciliary dyskinesia, primary, 40, MONDO:0032664
Green DNAH9 in Laterality disorders and isomerism


Level 2: Respiratory
Version 5.1
Latest signed off version: v5.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Primary ciliary dyskinesia, 40, 618300
Green DNAH9 in Respiratory ciliopathies including non-CF bronchiectasis


Level 2: Respiratory
Version 5.1
Latest signed off version: v5.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Ciliary dyskinesia, primary, 40, OMIM:618300
  • ciliary dyskinesia, primary, 40, MONDO:0032664
Green DNAH9 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.11
Latest signed off version: v7.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • DD-Gene2Phenotype
Phenotypes
  • Motile Cilia Defects and Situs Inversus
Green DNAH9 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • DD-Gene2Phenotype
    Phenotypes
    • Motile Cilia Defects and Situs Inversus