AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
Træk
Enlarged clitoris
Klinisk navn: Clitoral hypertrophy
Hypertrophy of the clitoris.
Resumé
- Også kaldet
- Clitoral enlargement, Clitoromegaly, Hypertrophic clitoris, Prominent clitoris
- Kropssystem
- Abnormality of the genitourinary system
AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
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/clitoral-hypertrophy.json"
page <- fromJSON(url)
page$trait$nameEnlarged clitorisHP:0008665
AtlasHvem vi hjælperVores videnskabProdukterResultater
Log indSpørgSekvenér dit genom↗
Læs de gener, der er knyttet til Enlarged clitoris, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test50 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.
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 10 of these genesDHX37GATA4HSD17B3MAP3K1NR5A1SRYAbout this report →
- Congenital Adrenal HyperplasiaReads 4 of these genesCYP11B1HSD3B2PORCYP11A1About this report →
- 46,XX Differences of Sex DevelopmentReads 3 of these genesNR5A1SRYRSPO1About this report →
Show 46 more reports
- Other Inherited LeukodystrophiesReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Rare Hereditary Peripheral NeuropathiesReads 16 of these genesFDXRPEX1PEX10PEX11BPEX12PEX13About this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- Kaufman Oculocerebrofacial SyndromeReads 1 of these genesUBE3BAbout this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Meier-Gorlin Syndrome 4Reads 1 of these genesCDT1About this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- Roberts SyndromeReads 1 of these genesESCO2About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- Inherited Neurodegenerative DisordersReads 18 of these genesWWOXPEX1PEX10PEX11BPEX12PEX13About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Hypertrophic CardiomyopathyReads 5 of these genesDHX37MAP3K1NR5A1SRYZFPM2About this report →
- LipodystrophyReads 2 of these genesAGPAT2BSCL2About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- Fraser SyndromeReads 1 of these genesFRAS1About this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 3 of these genesCOX7BHCCSNDUFB11About this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4BSCL2About this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR2PORAbout this report →
- Diabetes MellitusReads 2 of these genesGATA4BSCL2About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Coffin-Siris SyndromeReads 1 of these genesARID1BAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesWWOXPEX6About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCYP11B1About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesCEP152About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesFIG4BSCL2About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesTOE1About this report →
- Spinal Muscular AtrophyReads 1 of these genesBSCL2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesRSPO1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesVAC14About this report →
- Epilepsy (Full Panel)Reads 2 of these genesWWOXGAD1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesNR0B1About this report →
- Female InfertilityReads 1 of these genesNR5A1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesBSCL2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFB11About this report →
- Intellectual DisabilityReads 1 of these genesARID1BAbout this report →
Læs de gener, der er knyttet til Enlarged clitoris, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test69 gener knyttet til Enlarged clitoris
Ændringer i disse gener forårsager sjældne tilstande, hvor Enlarged clitoris 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 |
|---|---|---|
| ATIC5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Altid | I 2 tilstande |
| CACHD1cache domain containing 1 | Altid | I 1 tilstand |
| DONSONDNA replication fork stabilization factor DONSON | Altid | I 1 tilstand |
| FDXRferredoxin reductase | Altid | I 2 tilstande |
| FGFR2fibroblast growth factor receptor 2 | Altid | I 2 tilstande |
| INSRinsulin receptor | Altid | I 4 tilstande |
| DHX37DEAH-box helicase 37 | Meget ofte (80–99 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Meget ofte (80–99 %) | I 1 tilstand |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Meget ofte (80–99 %) | I 1 tilstand |
| KAT6Blysine acetyltransferase 6B | Meget ofte (80–99 %) | I 2 tilstande |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Meget ofte (80–99 %) | I 2 tilstande |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Meget ofte (80–99 %) | I 4 tilstande |
| SOX9SRY-box transcription factor 9 | Meget ofte (80–99 %) | I 1 tilstand |
| SRYsex determining region Y | Meget ofte (80–99 %) | I 2 tilstande |
| 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 |
| CCNQcyclin Q | Ofte (30–79 %) | I 2 tilstande |
| CDC45cell division cycle 45 | Ofte (30–79 %) | I 2 tilstande |
| CDC6cell division cycle 6 | Ofte (30–79 %) | I 1 tilstand |
| CDT1chromatin licensing and DNA replication factor 1 | Ofte (30–79 %) | I 1 tilstand |
| CEP152centrosomal protein 152 | Ofte (30–79 %) | I 1 tilstand |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Ofte (30–79 %) | I 2 tilstande |
| DHCR77-dehydrocholesterol reductase | Ofte (30–79 %) | I 1 tilstand |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Ofte (30–79 %) | I 2 tilstande |
| GMNNgeminin DNA replication inhibitor | Ofte (30–79 %) | I 1 tilstand |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Ofte (30–79 %) | I 1 tilstand |
| MED25mediator complex subunit 25 | Ofte (30–79 %) | I 1 tilstand |
| ORC1origin recognition complex subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| ORC4origin recognition complex subunit 4 | Ofte (30–79 %) | I 2 tilstande |
| ORC6origin recognition complex subunit 6 | Ofte (30–79 %) | I 2 tilstande |
| PEX1peroxisomal biogenesis factor 1 | Ofte (30–79 %) | I 2 tilstande |
| PEX10peroxisomal biogenesis factor 10 | Ofte (30–79 %) | I 1 tilstand |
| PEX11Bperoxisomal biogenesis factor 11 beta | Ofte (30–79 %) | I 1 tilstand |
| PEX12peroxisomal biogenesis factor 12 | Ofte (30–79 %) | I 1 tilstand |
| PEX13peroxisomal biogenesis factor 13 | Ofte (30–79 %) | I 1 tilstand |
| PEX14peroxisomal biogenesis factor 14 | Ofte (30–79 %) | I 1 tilstand |
| PEX16peroxisomal biogenesis factor 16 | Ofte (30–79 %) | I 1 tilstand |
Vis 29 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| PEX19peroxisomal biogenesis factor 19 | Ofte (30–79 %) | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Ofte (30–79 %) | I 2 tilstande |
| PEX26peroxisomal biogenesis factor 26 | Ofte (30–79 %) | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Ofte (30–79 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Ofte (30–79 %) | I 2 tilstande |
| PEX6peroxisomal biogenesis factor 6 | Ofte (30–79 %) | I 1 tilstand |
| PORcytochrome p450 oxidoreductase | Ofte (30–79 %) | I 1 tilstand |
| TOP2BDNA topoisomerase II beta | Ofte (30–79 %) | I 1 tilstand |
| ARandrogen receptor | Nogle gange (5–29 %) | I 1 tilstand |
| ARID1BAT-rich interaction domain 1B | Nogle gange (5–29 %) | I 1 tilstand |
| COX7Bcytochrome c oxidase subunit 7B | Nogle gange (5–29 %) | I 2 tilstande |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Nogle gange (5–29 %) | I 2 tilstande |
| FIG4FIG4 phosphoinositide 5-phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| GAD1glutamate decarboxylase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HCCSholocytochrome c synthase | Nogle gange (5–29 %) | I 2 tilstande |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Nogle gange (5–29 %) | I 2 tilstande |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Nogle gange (5–29 %) | I 1 tilstand |
| TOE1target of EGR1, exonuclease | Nogle gange (5–29 %) | I 1 tilstand |
| UBE3Bubiquitin protein ligase E3B | Nogle gange (5–29 %) | I 2 tilstande |
| VAC14VAC14 component of PIKFYVE complex | Nogle gange (5–29 %) | I 1 tilstand |
| AGPAT21-acylglycerol-3-phosphate O-acyltransferase 2 | Ikke registreret | I 1 tilstand |
| ATRATR checkpoint kinase | Ikke registreret | I 1 tilstand |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Ikke registreret | I 1 tilstand |
| CD96CD96 molecule | Ikke registreret | I 1 tilstand |
| FRAS1Fraser extracellular matrix complex subunit 1 | Ikke registreret | I 1 tilstand |
| RSPO1R-spondin 1 | Ikke registreret | I 1 tilstand |
| TALDO1transaldolase 1 | Ikke registreret | I 1 tilstand |
| TRAIPTRAF interacting protein | Ikke registreret | I 1 tilstand |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | 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
Log indSpørgSekvenér dit genom↗
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.
Fra 449 $
Gratis forsendelse · Resultater på 6–8 uger
