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Traits
Traits linked to DNAH9
dynein axonemal heavy chain 9
The Human Phenotype Ontology links 60 traits to DNAH9, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| All organs on wrong side of body | Often (30–79%) |
| Abnormal cardiovascular system morphology | Sometimes (5–29%) |
| Abnormality of the heart | Sometimes (5–29%) |
| Hole in center of heart | Sometimes (5–29%) |
| Interrupted inferior vena cava with azygous continuation | Sometimes (5–29%) |
| Levotransposition of the great arteries | Sometimes (5–29%) |
| Patent ductus arteriosus | Sometimes (5–29%) |
| Right aortic arch | Sometimes (5–29%) |
| Unbalanced atrioventricular canal defect | Sometimes (5–29%) |
| Abnormal inferior vena cava morphology | Rarely (1–4%) |
| Abnormal location of heart atrium | Rarely (1–4%) |
| Absent spleen | Rarely (1–4%) |
| Anomalous pulmonary venous return | Rarely (1–4%) |
| Atrial situs ambiguous | Rarely (1–4%) |
| Double outlet right ventricle | Rarely (1–4%) |
| Multiple small spleens | Rarely (1–4%) |
| Persistent left superior vena cava | Rarely (1–4%) |
| Transposition of the great arteries | Rarely (1–4%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Absent outer dynein arms | Always |
| Cough | Always |
| Abnormal sputum | Often (30–79%) |
| Neonatal respiratory distress | Often (30–79%) |
| Respiratory tract infection | Often (30–79%) |
| Wet cough | Often (30–79%) |
| Decreased nasal nitric oxide | Sometimes (5–29%) |
| Lithoptysis | Sometimes (5–29%) |
| Obstructive lung disease | Sometimes (5–29%) |
| Partial or complete collapse of part or entire lung | Sometimes (5–29%) |
| Peribronchovascular interstitial thickening | Sometimes (5–29%) |
| Permanent enlargement of the airways of the lungs | Sometimes (5–29%) |
| Pulmonary situs ambiguus | Sometimes (5–29%) |
| Reduced forced expiratory volume in one second | Sometimes (5–29%) |
| Reduced respiratory ciliary beating frequency | Sometimes (5–29%) |
| Wheezing | Sometimes (5–29%) |
| Respiratory failure | Rarely (1–4%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Absent sperm in semen | Always |
| Infertility | Always |
| Abnormal sperm motility | Often (30–79%) |
| Male infertility | Often (30–79%) |
| Abnormality of the genitourinary system | Sometimes (5–29%) |
| Female infertility | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Chronic rhinitis | Always |
| Chronic sinus disease | Always |
| Blockage of nose | Often (30–79%) |
| Nasal polyposis | Often (30–79%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Chronic infections of the middle ear | Often (30–79%) |
| Recurrent middle ear infection | Often (30–79%) |
| Conductive deafness | Sometimes (5–29%) |
| Hearing impairment | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Delayed speech and language development | Sometimes (5–29%) |
| Morphological central nervous system abnormality | Sometimes (5–29%) |
| Too much cerebrospinal fluid in the brain | Rarely (1–4%) |
| Ventriculomegaly | Rarely (1–4%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Recurrent sinus and lung infections | Often (30–79%) |
| Recurrent mycobacterial infections | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Clubbing of fingers and toes | Sometimes (5–29%) |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Intestinal malrotation | Rarely (1–4%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Rod-cone dystrophy | Rarely (1–4%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Abnormality of the skeletal system | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Left Isomerism | Sometimes (5–29%) |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to DNAH9 and how often each is seen. Find out more at hpo.jax.org.
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