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Trait
Psychomotor deterioration
Loss of previously present mental and motor abilities.
Summary
- Also called
- Psychomotor degeneration
- Body system
- Abnormality of the nervous system
Psychomotor deteriorationHP:0002361
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Read the genes linked to Psychomotor deterioration, and the rest of your genome, with one test.
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Get my Genome Test20 genes linked to Psychomotor deterioration
Changes in these genes cause rare conditions in which Psychomotor deterioration 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 |
|---|---|---|
| CLN3CLN3 lysosomal/endosomal transmembrane protein, battenin | Always | In 1 condition |
| PLP1proteolipid protein 1 | Always | In 1 condition |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Very often (80–99%) | In 1 condition |
| ATP6V1AATPase H+ transporting V1 subunit A | Very often (80–99%) | In 1 condition |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Very often (80–99%) | In 1 condition |
| PLA2G6phospholipase A2 group VI | Very often (80–99%) | In 1 condition |
| PPT1palmitoyl-protein thioesterase 1 | Very often (80–99%) | In 1 condition |
| COG2component of oligomeric golgi complex 2 | Often (30–79%) | In 1 condition |
| GALCgalactosylceramidase | Often (30–79%) | In 1 condition |
| PSAPprosaposin | Often (30–79%) | In 1 condition |
| KMT2Alysine methyltransferase 2A | Sometimes (5–29%) | In 1 condition |
| RNASEH1ribonuclease H1 | Sometimes (5–29%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sometimes (5–29%) | In 1 condition |
| GALK1galactokinase 1 | Rarely (1–4%) | In 1 condition |
| HEXAhexosaminidase subunit alpha | Not recorded | In 1 condition |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Not recorded | In 1 condition |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Not recorded | In 1 condition |
| PRRT2proline rich transmembrane protein 2 | Not recorded | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Not recorded | In 1 condition |
| SCN8Asodium voltage-gated channel alpha subunit 8 | 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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