Trait
Limited hair on end of eyebrow
Clinical name: Sparse lateral eyebrow
Decreased density/number and/or decreased diameter of lateral eyebrow hairs.
Summary
- Also called
- Lateral hypoplasia of eyebrows, Lateral thinning of eyebrows, Laterally sparse eyebrow, Laterally sparse eyebrows
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test36 genes linked to Limited hair on end of eyebrow
Changes in these genes cause rare conditions in which Limited hair on end of eyebrow 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 |
|---|---|---|
| DONSONDNA replication fork stabilization factor DONSON | Always | In 1 condition |
| HEPHL1hephaestin like 1 | Always | In 1 condition |
| IRX5iroquois homeobox 5 | Always | In 1 condition |
| KDF1keratinocyte differentiation factor 1 | Always | In 1 condition |
| KDM6Alysine demethylase 6A | Always | In 3 conditions |
| KMT2Dlysine methyltransferase 2D | Always | In 2 conditions |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Always | In 1 condition |
| TRPS1transcriptional repressor GATA binding 1 | Always | In 2 conditions |
| ATRATR checkpoint kinase | Very often (80–99%) | In 1 condition |
| COG6component of oligomeric golgi complex 6 | Often (30–79%) | In 1 condition |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Often (30–79%) | In 1 condition |
| KAT5lysine acetyltransferase 5 | Often (30–79%) | In 1 condition |
| MAN1B1mannosidase alpha class 1B member 1 | Often (30–79%) | In 1 condition |
| NECTIN1nectin cell adhesion molecule 1 | Often (30–79%) | In 1 condition |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Often (30–79%) | In 1 condition |
| PURApurine rich element binding protein A | Often (30–79%) | In 1 condition |
| TSHZ3teashirt zinc finger homeobox 3 | Often (30–79%) | In 1 condition |
| TWIST2twist family bHLH transcription factor 2 | Often (30–79%) | In 1 condition |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Often (30–79%) | In 1 condition |
| WDR26WD repeat domain 26 | Often (30–79%) | In 2 conditions |
| WLSWnt ligand secretion mediator | Often (30–79%) | In 1 condition |
| CDC42BPBCDC42 binding protein kinase beta | Sometimes (5–29%) | In 1 condition |
| H4C5H4 clustered histone 5 | Sometimes (5–29%) | In 1 condition |
| KMT5Blysine methyltransferase 5B | Sometimes (5–29%) | In 1 condition |
| KRT25keratin 25 | Sometimes (5–29%) | In 1 condition |
| KRT71keratin 71 | Sometimes (5–29%) | In 1 condition |
| KRT74keratin 74 | Sometimes (5–29%) | In 1 condition |
| LIPHlipase H | Sometimes (5–29%) | In 1 condition |
| LMBRD2LMBR1 domain containing 2 | Sometimes (5–29%) | In 1 condition |
| LPAR6lysophosphatidic acid receptor 6 | Sometimes (5–29%) | In 1 condition |
| MESDmesoderm development LRP chaperone | Sometimes (5–29%) | In 1 condition |
| PLXNA1plexin A1 | Sometimes (5–29%) | In 1 condition |
| EDARADDEDAR associated via death domain | Not recorded | In 1 condition |
| PIGKphosphatidylinositol glycan anchor biosynthesis class K | Not recorded | In 1 condition |
| PQBP1polyglutamine binding protein 1 | Not recorded | In 1 condition |
| TBX3T-box transcription factor 3 | 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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