Træk
True hermaphroditism
The presence of both ovarian and testicular tissues either in the same or in opposite gonads. Affected persons have ambiguous genitalia and may have 46,XX or 46,XY karyotypes or 46,XX/XY mosaicism.
Resumé
- Også kaldet
- Testicular and ovarian tissue present
- Kropssystem
- Abnormality of the genitourinary system
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Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/true-hermaphroditism.json"
page <- fromJSON(url)
page$trait$nameLæs de gener, der er knyttet til True hermaphroditism, og resten af dit genom, med én test.
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Bestil min Genome Test15 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.
- Meckel SyndromeReads 9 of these genesB9D1B9D2MKS1RPGRIP1LTCTN2TMEM107About this report →
- Joubert Syndrome And Related DisordersReads 15 of these genesB9D1B9D2CC2D2ACEP290CSPP1MKS1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 8 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
- 46,XX Differences of Sex DevelopmentReads 2 of these genesNR5A1SRYAbout this report →
Show 11 more reports
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 3 of these genesNR5A1SRYWT1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 2 of these genesCEP290RPGRIP1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesCEP290MKS1About this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesNR5A1SRYAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Female InfertilityReads 1 of these genesNR5A1About this report →
- Retinitis PigmentosaReads 1 of these genesCC2D2AAbout this report →
Læs de gener, der er knyttet til True hermaphroditism, og resten af dit genom, med én test.
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Bestil min Genome Test21 gener knyttet til True hermaphroditism
Ændringer i disse gener forårsager sjældne tilstande, hvor True hermaphroditism 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 |
|---|---|---|
| NR5A1nuclear receptor subfamily 5 group A member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SOX9SRY-box transcription factor 9 | Meget ofte (80–99 %) | I 2 tilstande |
| SRYsex determining region Y | Meget ofte (80–99 %) | I 2 tilstande |
| B9D1B9 domain containing 1 | Nogle gange (5–29 %) | I 1 tilstand |
| B9D2B9 domain containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CC2D2Acoiled-coil and C2 domain containing 2A | Nogle gange (5–29 %) | I 1 tilstand |
| CEP290centrosomal protein 290 | Nogle gange (5–29 %) | I 1 tilstand |
| CSPP1centrosome and spindle pole associated protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MKS1MKS transition zone complex subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RPGRIP1RPGR interacting protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RPGRIP1LRPGRIP1 like | Nogle gange (5–29 %) | I 1 tilstand |
| TCTN1tectonic family member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TCTN2tectonic family member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| TCTN3tectonic family member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM107transmembrane protein 107 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM216transmembrane protein 216 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM231transmembrane protein 231 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM237transmembrane protein 237 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM67transmembrane protein 67 | Nogle gange (5–29 %) | I 1 tilstand |
| TXNDC15thioredoxin domain containing 15 | Nogle gange (5–29 %) | I 1 tilstand |
| WT1WT1 transcription factor | 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.
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