Trait
Restrictive behavior
Behavior characterized by an abnormal limitation to a few interests and activities.
Summary
- Also called
- Restricted behavior, Restricted behaviour
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test18 genes linked to Restrictive behavior
Changes in these genes cause rare conditions in which Restrictive behavior is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| SLC13A1solute carrier family 13 member 1 | Always | In 1 condition |
| CHMP2Bcharged multivesicular body protein 2B | Very often (80–99%) | In 1 condition |
| GRNgranulin precursor | Very often (80–99%) | In 1 condition |
| MAPTmicrotubule associated protein tau | Very often (80–99%) | In 1 condition |
| PSEN1presenilin 1 | Very often (80–99%) | In 1 condition |
| SQSTM1sequestosome 1 | Very often (80–99%) | In 1 condition |
| TMEM106Btransmembrane protein 106B | Very often (80–99%) | In 1 condition |
| TREM2triggering receptor expressed on myeloid cells 2 | Very often (80–99%) | In 1 condition |
| VCPvalosin containing protein | Very often (80–99%) | In 1 condition |
| CDKL5cyclin dependent kinase like 5 | Often (30–79%) | In 1 condition |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Often (30–79%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Often (30–79%) | In 2 conditions |
| NTNG1netrin G1 | Often (30–79%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Often (30–79%) | In 1 condition |
| SPTBN1spectrin beta, non-erythrocytic 1 | Rarely (1–4%) | In 1 condition |
| NLGN3neuroligin 3 | Not recorded | In 2 conditions |
| NLGN4Xneuroligin 4 X-linked | Not recorded | In 2 conditions |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Not recorded | In 1 condition |
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.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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