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Traits
Traits linked to ODAD2
outer dynein arm docking complex subunit 2
The Human Phenotype Ontology links 51 traits to ODAD2, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Abnormal sputum | Often (30–79%) |
| Neonatal respiratory distress | Often (30–79%) |
| Permanent enlargement of the airways of the lungs | Often (30–79%) |
| Respiratory tract infection | Often (30–79%) |
| Wet cough | Often (30–79%) |
| 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%) |
| Pulmonary situs ambiguus | Sometimes (5–29%) |
| Wheezing | Sometimes (5–29%) |
| Respiratory failure | Rarely (1–4%) |
| Ciliary dyskinesia | Not recorded |
| Respiratory insufficiency due to defective ciliary clearance | Not recorded |
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%) |
| 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 head or neck
| Trait | How often it is seen |
|---|---|
| Blockage of nose | Often (30–79%) |
| Chronic rhinitis | Often (30–79%) |
| Chronic sinus disease | Often (30–79%) |
| Nasal polyposis | Often (30–79%) |
| Recurrent sinus disease | 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 genitourinary system
| Trait | How often it is seen |
|---|---|
| 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 the immune system
| Trait | How often it is seen |
|---|---|
| Chronic bronchitis | Often (30–79%) |
| Recurrent pneumonia | Often (30–79%) |
| Recurrent sinus and lung infections | Often (30–79%) |
| Recurrent mycobacterial infections | 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 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%) |
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 ODAD2 and how often each is seen. Find out more at hpo.jax.org.
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