AtlasTrait
Thick hair
Increased density of hairs, i.e., and elevated number of hairs per unit area.
Summary
- Also called
- Increased hair density, Increased follicular density
- Body system
- Abnormality of the integument
AtlasThis page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
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page <- fromJSON(url)
page$trait$nameRead the genes linked to Thick hair, and the rest of your genome, with one test.
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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.
- Cutis LaxaReads 4 of these genesATP6V0A2ATP6V1AATP6V1E1ATP7AAbout this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- Mucopolysaccharidosis-Plus SyndromeReads 1 of these genesVPS33AAbout this report →
Show 18 more reports
- Saul-Wilson SyndromeReads 1 of these genesCOG4About this report →
- Wiedemann-Steiner SyndromeReads 1 of these genesKMT2AAbout this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesSMC3About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Intellectual DisabilityReads 4 of these genesRUSC2VPS13BZFXASXL1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZFXAbout this report →
- Inherited IchthyosesReads 1 of these genesCLDN1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesCOG4ATP6V0A2About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesATP6V0A2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesNDUFAF6ATP7AAbout this report →
- Leigh SyndromeReads 1 of these genesNDUFAF6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesATP7AAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFAF6About this report →
- Epilepsy (Full Panel)Reads 1 of these genesATP6V1AAbout this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesATP7AAbout this report →
Read the genes linked to Thick hair, and the rest of your genome, with one test.
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Get my Genome Test21 genes linked to Thick hair
Changes in these genes cause rare conditions in which Thick 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 |
|---|---|---|
| COG4component of oligomeric golgi complex 4 | Always | In 2 conditions |
| KCNK4potassium two pore domain channel subfamily K member 4 | Always | In 1 condition |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | 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 |
| KMT2Alysine methyltransferase 2A | Very often (80–99%) | In 1 condition |
| AFF4ALF transcription elongation factor 4 | Often (30–79%) | In 2 conditions |
| INSRinsulin receptor | Often (30–79%) | In 1 condition |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Often (30–79%) | In 1 condition |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Often (30–79%) | In 1 condition |
| MSTO1misato mitochondrial distribution and morphology regulator 1 | Often (30–79%) | In 2 conditions |
| RUSC2RUN and SH3 domain containing 2 | Often (30–79%) | In 1 condition |
| VPS13Bvacuolar protein sorting 13 homolog B | Often (30–79%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Sometimes (5–29%) | In 1 condition |
| NEK1NIMA related kinase 1 | Sometimes (5–29%) | In 1 condition |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Sometimes (5–29%) | In 1 condition |
| ZFXzinc finger protein X-linked | Sometimes (5–29%) | In 1 condition |
| ASXL1ASXL transcriptional regulator 1 | Not recorded | In 1 condition |
| CLDN1claudin 1 | Not recorded | In 1 condition |
| SMC3structural maintenance of chromosomes 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 2026.10.19-9814e911.
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