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Traits
Traits linked to DPP9
dipeptidyl peptidase 9
The Human Phenotype Ontology links 55 traits to DPP9, 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 |
|---|---|
| Abnormality in area between air sacs in lung | Very often (80–99%) |
| Cough | Often (30–79%) |
| Crackles | Often (30–79%) |
| Decreased DLCO | Often (30–79%) |
| Exertional breathlessness | Often (30–79%) |
| Ground-glass opacification | Often (30–79%) |
| Honeycomb lung | Often (30–79%) |
| Permanent enlargement of the airways of the lungs | Often (30–79%) |
| Pulmonary scarring | Often (30–79%) |
| Reduced forced vital capacity | Often (30–79%) |
| Reticular pattern on pulmonary HRCT | Often (30–79%) |
| Subpleural honeycombing | Often (30–79%) |
| Usual interstitial pneumonia | Often (30–79%) |
| Orthodeoxia | Sometimes (5–29%) |
Abnormality of the immune system
| Trait | How often it is seen |
|---|---|
| Decreased immune function | Always |
| Recurrent bronchitis | Always |
| Recurrent infections | Always |
| Susceptibility to herpesvirus | Always |
| Allergy | Often (30–79%) |
| Asthma | Often (30–79%) |
| Baby eczema | Often (30–79%) |
| Eczema | Often (30–79%) |
Abnormality of the integument
| Trait | How often it is seen |
|---|---|
| Fair hair | Often (30–79%) |
| Hyperpigmented/hypopigmented macules | Often (30–79%) |
| Persistent blue color of hands or feet | Often (30–79%) |
| Dry skin | Sometimes (5–29%) |
| Lack of sweating | Sometimes (5–29%) |
| Poor wound healing | Sometimes (5–29%) |
| Premature graying of hair | Sometimes (5–29%) |
| Thickened skin | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Autism spectrum disorder | Often (30–79%) |
| Delayed speech and language development | Often (30–79%) |
| Slurred speech | Often (30–79%) |
| Specific learning disability | Often (30–79%) |
| Febrile seizure (within the age range of 3 months to 6 years) | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Low blood cell count | Always |
| Low number of red blood cells or hemoglobin | Always |
| Petechiae | Always |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Acid reflux | Often (30–79%) |
| Feeding difficulties | Often (30–79%) |
| Inguinal hernia | Often (30–79%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Faltering weight | Always |
| Proportionate short stature | Always |
| Prenatal growth deficiency | Often (30–79%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Downward slanting of the opening between the eyelids | Often (30–79%) |
| Broad forehead | Sometimes (5–29%) |
Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Hypospadias | Sometimes (5–29%) |
| Undescended testes | Sometimes (5–29%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Fatigue | Often (30–79%) |
| Decreased ability to exercise | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Clubbing of fingers | Often (30–79%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| Pulmonic regurgitation | Sometimes (5–29%) |
Abnormality of the ear
| Trait | How often it is seen |
|---|---|
| Recurrent middle ear infection | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Missing part of vertebrae | Always |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Episodic fever | Always |
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 DPP9 and how often each is seen. Find out more at hpo.jax.org.
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