Tratto
Bilateral cryptorchidism
Absence of both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the scrotum.
Riepilogo
- Detto anche
- Cryptorchidism, bilateral
- Sistema corporeo
- Abnormality of the genitourinary system
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page$trait$nameLeggi i geni collegati a Bilateral cryptorchidism e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test47 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.
- Joubert Syndrome And Related DisordersReads 8 of these genesCPLANE1FAM149B1KIF7OFD1PDE6DTCTN3About this report →
- 3MC Syndrome 1 (MASP1)Reads 1 of these genesMASP1About this report →
- Aarskog-Scott SyndromeReads 1 of these genesFGD1About this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
Show 43 more reports
- DCMA Syndrome (3-Methylglutaconic Aciduria Type 5)Reads 1 of these genesDNAJC19About this report →
- Elsahy-Waters SyndromeReads 1 of these genesCDH11About this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Neurooculocardiogenitourinary Syndrome (WDR37)Reads 1 of these genesWDR37About this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- Orofaciodigital Syndrome Type 14Reads 1 of these genesC2CD3About this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 4 of these genesAMHAMHR2ARSRYAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Syndromic CraniosynostosisReads 3 of these genesTWIST1KAT6AMEGF8About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesSMARCAL1About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Cutis LaxaReads 2 of these genesATP6V1AATP6V1E1About this report →
- 46,XX Differences of Sex DevelopmentReads 1 of these genesSRYAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Intellectual DisabilityReads 7 of these genesASH1LCREBBPEP300KLHL15KAT6ARPL10About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesKCNK3About this report →
- Colorectal Cancer & PolyposisReads 1 of these genesPOLEAbout this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesCYP17A1About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesMRAPAbout this report →
- Retinitis PigmentosaReads 3 of these genesIFT172OFD1TOPORSAbout this report →
- Meckel SyndromeReads 1 of these genesTMEM231About this report →
- DNA Repair DiseaseReads 2 of these genesERCC6GTF2H5About this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesTMEM216TMEM231About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesLSSAbout this report →
- Congenital MyopathiesReads 1 of these genesRYR1About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesIFT172About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesLSSAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesASH1LAbout this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesARTMEM216TMEM231FARS2About this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesSRYAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesFARS2About this report →
- Leigh SyndromeReads 1 of these genesFARS2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesFARS2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesATP6V1AAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSMARCAL1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesFARS2About this report →
Leggi i geni collegati a Bilateral cryptorchidism e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test62 geni collegati a Bilateral cryptorchidism
Alterazioni in questi geni causano malattie rare in cui si osserva Bilateral cryptorchidism. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ALX4ALX homeobox 4 | Sempre | In 1 condizione |
| AMHanti-Mullerian hormone | Sempre | In 1 condizione |
| AMHR2anti-Mullerian hormone receptor type 2 | Sempre | In 1 condizione |
| ASH1LASH1 like histone lysine methyltransferase | Sempre | In 1 condizione |
| CDH11cadherin 11 | Sempre | In 1 condizione |
| CREBBPCREB binding lysine acetyltransferase | Sempre | In 1 condizione |
| DHRS3dehydrogenase/reductase 3 | Sempre | In 1 condizione |
| EP300EP300 lysine acetyltransferase | Sempre | In 1 condizione |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Sempre | In 1 condizione |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Sempre | In 1 condizione |
| GTF2H5general transcription factor IIH subunit 5 | Sempre | In 1 condizione |
| HYAL2hyaluronidase 2 | Sempre | In 1 condizione |
| KCNK3potassium two pore domain channel subfamily K member 3 | Sempre | In 1 condizione |
| KDM2Blysine demethylase 2B | Sempre | In 1 condizione |
| KLHL15kelch like family member 15 | Sempre | In 1 condizione |
| MCM5minichromosome maintenance complex component 5 | Sempre | In 1 condizione |
| MRAPmelanocortin 2 receptor accessory protein | Sempre | In 1 condizione |
| PAICSphosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthase | Sempre | In 1 condizione |
| POLEDNA polymerase epsilon, catalytic subunit | Sempre | In 1 condizione |
| POLR1ARNA polymerase I subunit A | Sempre | In 1 condizione |
| RYR1ryanodine receptor 1 | Sempre | In 1 condizione |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Sempre | In 1 condizione |
| TM2D3TM2 domain containing 3 | Sempre | In 1 condizione |
| TOP2BDNA topoisomerase II beta | Sempre | In 1 condizione |
| TWIST1twist family bHLH transcription factor 1 | Sempre | In 1 condizione |
| WDR37WD repeat domain 37 | Sempre | In 1 condizione |
| ARandrogen receptor | Molto spesso (80–99%) | In 2 condizioni |
| ATP6V1AATPase H+ transporting V1 subunit A | Spesso (30–79%) | In 1 condizione |
| C2CD3C2 domain containing 3 centriole elongation regulator | Spesso (30–79%) | In 1 condizione |
| COLEC10collectin subfamily member 10 | Spesso (30–79%) | In 1 condizione |
| COLEC11collectin subfamily member 11 | Spesso (30–79%) | In 1 condizione |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Spesso (30–79%) | In 1 condizione |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Spesso (30–79%) | In 1 condizione |
| FAM149B1family with sequence similarity 149 member B1 | Spesso (30–79%) | In 1 condizione |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Spesso (30–79%) | In 1 condizione |
| IFT172intraflagellar transport 172 | Spesso (30–79%) | In 1 condizione |
| IGBP1immunoglobulin binding protein 1 | Spesso (30–79%) | In 1 condizione |
| KAT6Alysine acetyltransferase 6A | Spesso (30–79%) | In 1 condizione |
| KIAA0753KIAA0753 | Spesso (30–79%) | In 1 condizione |
| KIF7kinesin family member 7 | Spesso (30–79%) | In 1 condizione |
Mostra altri 22 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| MASP1MBL associated serine protease 1 | Spesso (30–79%) | In 1 condizione |
| MEGF8multiple EGF like domains 8 | Spesso (30–79%) | In 1 condizione |
| NFIXnuclear factor I X | Spesso (30–79%) | In 1 condizione |
| NOTCH3notch receptor 3 | Spesso (30–79%) | In 1 condizione |
| ODC1ornithine decarboxylase 1 | Spesso (30–79%) | In 1 condizione |
| OFD1OFD1 centriole and centriolar satellite protein | Spesso (30–79%) | In 1 condizione |
| PDE6Dphosphodiesterase 6D | Spesso (30–79%) | In 1 condizione |
| RPL10ribosomal protein L10 | Spesso (30–79%) | In 1 condizione |
| SRYsex determining region Y | Spesso (30–79%) | In 1 condizione |
| TCTN3tectonic family member 3 | Spesso (30–79%) | In 1 condizione |
| TMEM216transmembrane protein 216 | Spesso (30–79%) | In 1 condizione |
| TMEM231transmembrane protein 231 | Spesso (30–79%) | In 1 condizione |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Spesso (30–79%) | In 1 condizione |
| VPS50VPS50 subunit of EARP/GARPII complex | Spesso (30–79%) | In 1 condizione |
| ZBTB20zinc finger and BTB domain containing 20 | Spesso (30–79%) | In 2 condizioni |
| ZRSR2zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | Spesso (30–79%) | In 1 condizione |
| DNAJC19DnaJ heat shock protein family (Hsp40) member C19 | A volte (5–29%) | In 1 condizione |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | A volte (5–29%) | In 1 condizione |
| LSSlanosterol synthase | A volte (5–29%) | In 1 condizione |
| NONOnon-POU domain containing octamer binding | A volte (5–29%) | In 1 condizione |
| RIPK4receptor interacting serine/threonine kinase 4 | A volte (5–29%) | In 1 condizione |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.19-9814e911.
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