Trait
Mild short stature
A mild degree of short stature, more than -2 SD but not more than -3 SD from mean corrected for age and sex.
Summary
- Also called
- short stature, mild
- Body system
- Growth abnormality
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test23 genes linked to Mild short stature
Changes in these genes cause rare conditions in which Mild short stature 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 |
|---|---|---|
| AGO1argonaute RISC component 1 | Always | In 1 condition |
| CANT1calcium activated nucleotidase 1 | Always | In 1 condition |
| CHST11carbohydrate sulfotransferase 11 | Always | In 1 condition |
| COMPcartilage oligomeric matrix protein | Always | In 1 condition |
| LBRlamin B receptor | Always | In 2 conditions |
| ZMYM3zinc finger MYM-type containing 3 | Always | In 1 condition |
| CTNNB1catenin beta 1 | Very often (80–99%) | In 1 condition |
| EVCEvC ciliary complex subunit 1 | Very often (80–99%) | In 2 conditions |
| EVC2EvC ciliary complex subunit 2 | Very often (80–99%) | In 2 conditions |
| MATN3matrilin 3 | Often (30–79%) | In 1 condition |
| PCGF2polycomb group ring finger 2 | Often (30–79%) | In 1 condition |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Often (30–79%) | In 1 condition |
| CYP19A1cytochrome P450 family 19 subfamily A member 1 | Sometimes (5–29%) | In 1 condition |
| PDE4Dphosphodiesterase 4D | Sometimes (5–29%) | In 1 condition |
| CAMK2Gcalcium/calmodulin dependent protein kinase II gamma | Not recorded | In 1 condition |
| COL10A1collagen type X alpha 1 chain | Not recorded | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Not recorded | In 1 condition |
| COL9A2collagen type IX alpha 2 chain | Not recorded | In 1 condition |
| COL9A3collagen type IX alpha 3 chain | Not recorded | In 1 condition |
| DOCK3dedicator of cytokinesis 3 | Not recorded | In 1 condition |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Not recorded | In 1 condition |
| IDSiduronate 2-sulfatase | Not recorded | In 1 condition |
| RTTNrotatin | 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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