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Traits
Traits linked to MFAP5
microfibril associated protein 5
The Human Phenotype Ontology links 49 traits to MFAP5, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the cardiovascular system
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Abnormality of connective tissue | Very often (80–99%) |
| Abnormality of the sternum | Sometimes (5–29%) |
| Funnel chest | Sometimes (5–29%) |
| Pigeon chest | Sometimes (5–29%) |
| Scoliosis | Sometimes (5–29%) |
Abnormality of the respiratory system
| Trait | How often it is seen |
|---|---|
| Exertional breathlessness | Often (30–79%) |
| Paroxysmal dyspnea | Often (30–79%) |
| Collapsed lung | Sometimes (5–29%) |
| Coughing up blood | Sometimes (5–29%) |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| High palate | Often (30–79%) |
| High, narrow palate | Sometimes (5–29%) |
| Receding chin | Sometimes (5–29%) |
Abnormality of blood and blood-forming tissues
| Trait | How often it is seen |
|---|---|
| Bruising susceptibility | Sometimes (5–29%) |
| Subarachnoid hemorrhage | Sometimes (5–29%) |
Abnormality of limbs
| Trait | How often it is seen |
|---|---|
| Long slender fingers | Often (30–79%) |
| Dropped arches | Sometimes (5–29%) |
Abnormality of the eye
| Trait | How often it is seen |
|---|---|
| Abnormality of the iris | Often (30–79%) |
| Wide-set eyes | Sometimes (5–29%) |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Tall stature | Sometimes (5–29%) |
| Disproportionate tall stature | Not recorded |
Abnormality of the digestive system
| Trait | How often it is seen |
|---|---|
| Inguinal hernia | Sometimes (5–29%) |
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Dural ectasia | Often (30–79%) |
Constitutional symptom
| Trait | How often it is seen |
|---|---|
| Chest pain | Often (30–79%) |
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 MFAP5 and how often each is seen. Find out more at hpo.jax.org.
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