Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Traits
Traits linked to NCAPD2
non-SMC condensin I complex subunit D2
The Human Phenotype Ontology links 7 traits to NCAPD2, by body system: features seen in people with one of the gene's rare conditions.
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Abnormality of the nervous system
| Trait | How often it is seen |
|---|---|
| Absent speech development | Always |
| Autism spectrum disorder | Always |
| IQ between 34 and 49 | Always |
Abnormality of head or neck
| Trait | How often it is seen |
|---|---|
| Sloping forehead | Always |
| Small head present at birth | Always |
Growth abnormality
| Trait | How often it is seen |
|---|---|
| Short stature | Always |
| Small for gestational age | 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 NCAPD2 and how often each is seen. Find out more at hpo.jax.org.
Who We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks