Trait
Excessive face hair
Clinical name: Facial hirsutism
Excess facial hair.
Summary
- Body system
- Abnormality of the integument
This page as data
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library(jsonlite)
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page$trait$nameRead the genes linked to Excessive face hair, and the rest of your genome, with one test.
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Get my Genome Test9 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
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- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesWNT4About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 1 of these genesGNSAbout this report →
Show 5 more reports
- Hepatic Porphyria DisordersReads 1 of these genesCPOXAbout this report →
- PorphyriaReads 1 of these genesCPOXAbout this report →
- Female InfertilityReads 2 of these genesWNT4TP63About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGNSAbout this report →
Read the genes linked to Excessive face hair, and the rest of your genome, with one test.
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Get my Genome Test8 genes linked to Excessive face hair
Changes in these genes cause rare conditions in which Excessive face hair 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 |
|---|---|---|
| GNSglucosamine (N-acetyl)-6-sulfatase | Always | In 1 condition |
| WNT4Wnt family member 4 | Very often (80–99%) | In 1 condition |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Often (30–79%) | In 1 condition |
| TP63tumor protein p63 | Often (30–79%) | In 1 condition |
| AFF4ALF transcription elongation factor 4 | Sometimes (5–29%) | In 1 condition |
| CPOXcoproporphyrinogen oxidase | Sometimes (5–29%) | In 1 condition |
| PEPDpeptidase D | Not recorded | In 1 condition |
| TBX15T-box transcription factor 15 | 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.
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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 2026.10.19-9814e911.
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