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Trait
Limited armpit hair
Clinical name: Sparse axillary hair
Reduced number or density of axillary hair.
Summary
- Also called
- Little underarm hair, sparse to absent axillary hair
- Body system
- Abnormality of the integument
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Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/sparse-axillary-hair.json"
page <- fromJSON(url)
page$trait$nameLimited armpit hairHP:0002215
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Get my Genome Test38 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.
- Hypogonadotropic HypogonadismReads 19 of these genesANOS1CHD7FEZF1FGF17FGF8FGFR1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 8 of these genesDHX37GATA4MAP3K1NR5A1SRYWT1About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 4 of these genesLIPHRPL21LPAR6APCDD1About this report →
- 46,XX Differences of Sex DevelopmentReads 2 of these genesNR5A1SRYAbout this report →
Show 34 more reports
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Scalp-Ear-Nipple SyndromeReads 1 of these genesKCTD1About this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- Ulnar-Mammary SyndromeReads 1 of these genesTBX3About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 3 of these genesADAMTS3CCBE1FAT4About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Hypertrophic CardiomyopathyReads 5 of these genesDHX37MAP3K1NR5A1SRYZFPM2About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Ectodermal DysplasiasReads 2 of these genesGJB6TP63About this report →
- Epidermolysis BullosaReads 2 of these genesCOL17A1ITGB4About this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesCYB5AAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAXIN2About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesCYP17A1About this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- Type I InterferonopathiesReads 1 of these genesPSMB8About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Female InfertilityReads 2 of these genesNR5A1TP63About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesCOL17A1About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Diabetes MellitusReads 1 of these genesGATA4About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPSMB8About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJB6About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesWWOXAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesWWOXARAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesGJB6About this report →
- Epilepsy (Full Panel)Reads 1 of these genesWWOXAbout this report →
- Intellectual DisabilityReads 1 of these genesWDR11About this report →
Read the genes linked to Limited armpit hair, and the rest of your genome, with one test.
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Get my Genome Test60 genes linked to Limited armpit hair
Changes in these genes cause rare conditions in which Limited armpit 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 |
|---|---|---|
| ANOS1anosmin 1 | Always | In 1 condition |
| AXLAXL receptor tyrosine kinase | Always | In 1 condition |
| CCDC141coiled-coil domain containing 141 | Always | In 1 condition |
| CHD7chromodomain helicase DNA binding protein 7 | Always | In 1 condition |
| DSC3desmocollin 3 | Always | In 1 condition |
| DUSP6dual specificity phosphatase 6 | Always | In 1 condition |
| FEZF1FEZ family zinc finger 1 | Always | In 1 condition |
| FGF17fibroblast growth factor 17 | Always | In 1 condition |
| FGF8fibroblast growth factor 8 | Always | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Always | In 1 condition |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Always | In 1 condition |
| GNRH1gonadotropin releasing hormone 1 | Always | In 1 condition |
| GNRHRgonadotropin releasing hormone receptor | Always | In 1 condition |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Always | In 1 condition |
| KCTD1potassium channel tetramerization domain containing 1 | Always | In 1 condition |
| KISS1KiSS-1 metastasis suppressor | Always | In 1 condition |
| KISS1RKISS1 receptor | Always | In 1 condition |
| LHBluteinizing hormone subunit beta | Always | In 1 condition |
| LIPHlipase H | Always | In 1 condition |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Always | In 1 condition |
| PROK2prokineticin 2 | Always | In 1 condition |
| PROKR2prokineticin receptor 2 | Always | In 1 condition |
| SEMA3Asemaphorin 3A | Always | In 1 condition |
| SEMA3Esemaphorin 3E | Always | In 1 condition |
| SOX10SRY-box transcription factor 10 | Always | In 1 condition |
| SPRY4sprouty RTK signaling antagonist 4 | Always | In 1 condition |
| SRA1steroid receptor RNA activator 1 | Always | In 1 condition |
| TAC3tachykinin precursor 3 | Always | In 1 condition |
| TACR3tachykinin receptor 3 | Always | In 1 condition |
| WDR11WD repeat domain 11 | Always | In 1 condition |
| CYB5Acytochrome b5 type A | Very often (80–99%) | In 1 condition |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Very often (80–99%) | In 1 condition |
| DHX37DEAH-box helicase 37 | Very often (80–99%) | In 1 condition |
| FSHBfollicle stimulating hormone subunit beta | Very often (80–99%) | In 1 condition |
| GATA4GATA binding protein 4 | Very often (80–99%) | In 1 condition |
| HLA-DRAmajor histocompatibility complex, class II, DR alpha | Very often (80–99%) | In 1 condition |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Very often (80–99%) | In 2 conditions |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Very often (80–99%) | In 1 condition |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Very often (80–99%) | In 1 condition |
| RPL21ribosomal protein L21 | Very often (80–99%) | In 1 condition |
Show 20 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| SOX9SRY-box transcription factor 9 | Very often (80–99%) | In 1 condition |
| SRYsex determining region Y | Very often (80–99%) | In 1 condition |
| VAMP7vesicle associated membrane protein 7 | Very often (80–99%) | In 1 condition |
| WT1WT1 transcription factor | Very often (80–99%) | In 1 condition |
| WWOXWW domain containing oxidoreductase | Very often (80–99%) | In 1 condition |
| ZFPM2zinc finger protein, FOG family member 2 | Very often (80–99%) | In 1 condition |
| ARandrogen receptor | Often (30–79%) | In 2 conditions |
| COL17A1collagen type XVII alpha 1 chain | Often (30–79%) | In 1 condition |
| ITGB4integrin subunit beta 4 | Often (30–79%) | In 1 condition |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Sometimes (5–29%) | In 1 condition |
| AXIN2axin 2 | Sometimes (5–29%) | In 1 condition |
| CCBE1collagen and calcium binding EGF domains 1 | Sometimes (5–29%) | In 1 condition |
| FAT4FAT atypical cadherin 4 | Sometimes (5–29%) | In 1 condition |
| GJB6gap junction protein beta 6 | Sometimes (5–29%) | In 1 condition |
| LPAR6lysophosphatidic acid receptor 6 | Sometimes (5–29%) | In 1 condition |
| PSMB8proteasome 20S subunit beta 8 | Sometimes (5–29%) | In 1 condition |
| APCDD1APC down-regulated 1 | Not recorded | In 1 condition |
| ORC6origin recognition complex subunit 6 | Not recorded | In 1 condition |
| TBX3T-box transcription factor 3 | Not recorded | In 1 condition |
| TP63tumor protein p63 | Not recorded | In 2 conditions |
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 2026.10.21-777c9289.
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