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Træk
Sparse pubic hair
Reduced number or density of pubic hair.
Resumé
- Også kaldet
- Decreased sexual hair, sparse to absent pubic hair
- Kropssystem
- Abnormality of the integument
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/sparse-pubic-hair.json"
page <- fromJSON(url)
page$trait$nameSparse pubic hairHP:0002225
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Læs de gener, der er knyttet til Sparse pubic hair, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test36 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 →
- Female InfertilityReads 12 of these genesNR5A1BMP15BNC1FIGLAFSHRMRPS22About this report →
- 46,XX Differences of Sex DevelopmentReads 2 of these genesNR5A1SRYAbout this report →
Show 32 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 →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Polycystic Ovary SyndromeReads 1 of these genesFSHRAbout 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 →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 3 of these genesRPL21LSSAPCDD1About 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 →
- 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 →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesCOL17A1About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesLSSAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Nephrotic SyndromeReads 1 of these genesNUP107About this report →
- Diabetes MellitusReads 1 of these genesGATA4About 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 →
- Primary Mitochondrial DiseaseReads 1 of these genesMRPS22About this report →
- Epilepsy (Full Panel)Reads 1 of these genesWWOXAbout this report →
- Intellectual DisabilityReads 1 of these genesWDR11About this report →
Læs de gener, der er knyttet til Sparse pubic hair, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test66 gener knyttet til Sparse pubic hair
Ændringer i disse gener forårsager sjældne tilstande, hvor Sparse pubic hair ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ANOS1anosmin 1 | Altid | I 2 tilstande |
| AXLAXL receptor tyrosine kinase | Altid | I 1 tilstand |
| CCDC141coiled-coil domain containing 141 | Altid | I 1 tilstand |
| CHD7chromodomain helicase DNA binding protein 7 | Altid | I 1 tilstand |
| DUSP6dual specificity phosphatase 6 | Altid | I 1 tilstand |
| FEZF1FEZ family zinc finger 1 | Altid | I 1 tilstand |
| FGF17fibroblast growth factor 17 | Altid | I 1 tilstand |
| FGF8fibroblast growth factor 8 | Altid | I 1 tilstand |
| FGFR1fibroblast growth factor receptor 1 | Altid | I 1 tilstand |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Altid | I 1 tilstand |
| GNRH1gonadotropin releasing hormone 1 | Altid | I 1 tilstand |
| GNRHRgonadotropin releasing hormone receptor | Altid | I 1 tilstand |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Altid | I 1 tilstand |
| KCTD1potassium channel tetramerization domain containing 1 | Altid | I 1 tilstand |
| KISS1KiSS-1 metastasis suppressor | Altid | I 1 tilstand |
| KISS1RKISS1 receptor | Altid | I 1 tilstand |
| LHBluteinizing hormone subunit beta | Altid | I 1 tilstand |
| MDM2MDM2 proto-oncogene | Altid | I 1 tilstand |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Altid | I 1 tilstand |
| PROK2prokineticin 2 | Altid | I 1 tilstand |
| PROKR2prokineticin receptor 2 | Altid | I 1 tilstand |
| SEMA3Asemaphorin 3A | Altid | I 1 tilstand |
| SEMA3Esemaphorin 3E | Altid | I 1 tilstand |
| SOX10SRY-box transcription factor 10 | Altid | I 1 tilstand |
| SPRY4sprouty RTK signaling antagonist 4 | Altid | I 1 tilstand |
| SRA1steroid receptor RNA activator 1 | Altid | I 1 tilstand |
| TAC3tachykinin precursor 3 | Altid | I 1 tilstand |
| TACR3tachykinin receptor 3 | Altid | I 1 tilstand |
| WDR11WD repeat domain 11 | Altid | I 1 tilstand |
| CYB5Acytochrome b5 type A | Meget ofte (80–99 %) | I 1 tilstand |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| DHX37DEAH-box helicase 37 | Meget ofte (80–99 %) | I 1 tilstand |
| FSHBfollicle stimulating hormone subunit beta | Meget ofte (80–99 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Meget ofte (80–99 %) | I 1 tilstand |
| HLA-DRAmajor histocompatibility complex, class II, DR alpha | Meget ofte (80–99 %) | I 1 tilstand |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| RPL21ribosomal protein L21 | Meget ofte (80–99 %) | I 1 tilstand |
| SOX9SRY-box transcription factor 9 | Meget ofte (80–99 %) | I 1 tilstand |
Vis 26 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SRYsex determining region Y | Meget ofte (80–99 %) | I 1 tilstand |
| VAMP7vesicle associated membrane protein 7 | Meget ofte (80–99 %) | I 1 tilstand |
| WT1WT1 transcription factor | Meget ofte (80–99 %) | I 1 tilstand |
| WWOXWW domain containing oxidoreductase | Meget ofte (80–99 %) | I 1 tilstand |
| ZFPM2zinc finger protein, FOG family member 2 | Meget ofte (80–99 %) | I 1 tilstand |
| ARandrogen receptor | Ofte (30–79 %) | I 2 tilstande |
| BMP15bone morphogenetic protein 15 | Ofte (30–79 %) | I 1 tilstand |
| BNC1basonuclin zinc finger protein 1 | Ofte (30–79 %) | I 1 tilstand |
| COL17A1collagen type XVII alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| FIGLAfolliculogenesis specific bHLH transcription factor | Ofte (30–79 %) | I 1 tilstand |
| FSHRfollicle stimulating hormone receptor | Ofte (30–79 %) | I 1 tilstand |
| ITGB4integrin subunit beta 4 | Ofte (30–79 %) | I 1 tilstand |
| LSSlanosterol synthase | Ofte (30–79 %) | I 1 tilstand |
| MRPS22mitochondrial ribosomal protein S22 | Ofte (30–79 %) | I 1 tilstand |
| MSH4mutS homolog 4 | Ofte (30–79 %) | I 1 tilstand |
| NUP107nucleoporin 107 | Ofte (30–79 %) | I 1 tilstand |
| POLR3HRNA polymerase III subunit H | Ofte (30–79 %) | I 1 tilstand |
| PSMC3IPPSMC3 interacting protein | Ofte (30–79 %) | I 1 tilstand |
| SPIDRscaffold protein involved in DNA repair | Ofte (30–79 %) | I 1 tilstand |
| ZSWIM7zinc finger SWIM-type containing 7 | Ofte (30–79 %) | I 1 tilstand |
| GJB6gap junction protein beta 6 | Nogle gange (5–29 %) | I 1 tilstand |
| PPP2R3Cprotein phosphatase 2 regulatory subunit B''gamma | Nogle gange (5–29 %) | I 1 tilstand |
| APCDD1APC down-regulated 1 | Ikke registreret | I 1 tilstand |
| FOXL2forkhead box L2 | Ikke registreret | I 1 tilstand |
| ORC6origin recognition complex subunit 6 | Ikke registreret | I 1 tilstand |
| TP63tumor protein p63 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
AtlasHvem vi hjælperVores videnskabProdukterResultater
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From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
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