Atlas우리가 돕는 분들과학적 근거제품연구 성과
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형질
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.
요약
- 다른 명칭
- Cryptorchidism, bilateral
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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page$trait$nameBilateral cryptorchidismHP:0008689
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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Bilateral cryptorchidism과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
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내 Genome Test 받기47 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 →
Bilateral cryptorchidism과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기연관 유전자 62개: Bilateral cryptorchidism
이 유전자들의 변화는 Bilateral cryptorchidism 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| ALX4ALX homeobox 4 | 항상 | 질환 1개에서 나타남 |
| AMHanti-Mullerian hormone | 항상 | 질환 1개에서 나타남 |
| AMHR2anti-Mullerian hormone receptor type 2 | 항상 | 질환 1개에서 나타남 |
| ASH1LASH1 like histone lysine methyltransferase | 항상 | 질환 1개에서 나타남 |
| CDH11cadherin 11 | 항상 | 질환 1개에서 나타남 |
| CREBBPCREB binding lysine acetyltransferase | 항상 | 질환 1개에서 나타남 |
| DHRS3dehydrogenase/reductase 3 | 항상 | 질환 1개에서 나타남 |
| EP300EP300 lysine acetyltransferase | 항상 | 질환 1개에서 나타남 |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | 항상 | 질환 1개에서 나타남 |
| FGD1FYVE, RhoGEF and PH domain containing 1 | 항상 | 질환 1개에서 나타남 |
| GTF2H5general transcription factor IIH subunit 5 | 항상 | 질환 1개에서 나타남 |
| HYAL2hyaluronidase 2 | 항상 | 질환 1개에서 나타남 |
| KCNK3potassium two pore domain channel subfamily K member 3 | 항상 | 질환 1개에서 나타남 |
| KDM2Blysine demethylase 2B | 항상 | 질환 1개에서 나타남 |
| KLHL15kelch like family member 15 | 항상 | 질환 1개에서 나타남 |
| MCM5minichromosome maintenance complex component 5 | 항상 | 질환 1개에서 나타남 |
| MRAPmelanocortin 2 receptor accessory protein | 항상 | 질환 1개에서 나타남 |
| PAICSphosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthase | 항상 | 질환 1개에서 나타남 |
| POLEDNA polymerase epsilon, catalytic subunit | 항상 | 질환 1개에서 나타남 |
| POLR1ARNA polymerase I subunit A | 항상 | 질환 1개에서 나타남 |
| RYR1ryanodine receptor 1 | 항상 | 질환 1개에서 나타남 |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | 항상 | 질환 1개에서 나타남 |
| TM2D3TM2 domain containing 3 | 항상 | 질환 1개에서 나타남 |
| TOP2BDNA topoisomerase II beta | 항상 | 질환 1개에서 나타남 |
| TWIST1twist family bHLH transcription factor 1 | 항상 | 질환 1개에서 나타남 |
| WDR37WD repeat domain 37 | 항상 | 질환 1개에서 나타남 |
| ARandrogen receptor | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| ATP6V1AATPase H+ transporting V1 subunit A | 자주 (30–79%) | 질환 1개에서 나타남 |
| C2CD3C2 domain containing 3 centriole elongation regulator | 자주 (30–79%) | 질환 1개에서 나타남 |
| COLEC10collectin subfamily member 10 | 자주 (30–79%) | 질환 1개에서 나타남 |
| COLEC11collectin subfamily member 11 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| FAM149B1family with sequence similarity 149 member B1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IFT172intraflagellar transport 172 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IGBP1immunoglobulin binding protein 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| KAT6Alysine acetyltransferase 6A | 자주 (30–79%) | 질환 1개에서 나타남 |
| KIAA0753KIAA0753 | 자주 (30–79%) | 질환 1개에서 나타남 |
| KIF7kinesin family member 7 | 자주 (30–79%) | 질환 1개에서 나타남 |
유전자 22개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| MASP1MBL associated serine protease 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MEGF8multiple EGF like domains 8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| NFIXnuclear factor I X | 자주 (30–79%) | 질환 1개에서 나타남 |
| NOTCH3notch receptor 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ODC1ornithine decarboxylase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| OFD1OFD1 centriole and centriolar satellite protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| PDE6Dphosphodiesterase 6D | 자주 (30–79%) | 질환 1개에서 나타남 |
| RPL10ribosomal protein L10 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SRYsex determining region Y | 자주 (30–79%) | 질환 1개에서 나타남 |
| TCTN3tectonic family member 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TMEM216transmembrane protein 216 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TMEM231transmembrane protein 231 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | 자주 (30–79%) | 질환 1개에서 나타남 |
| VPS50VPS50 subunit of EARP/GARPII complex | 자주 (30–79%) | 질환 1개에서 나타남 |
| ZBTB20zinc finger and BTB domain containing 20 | 자주 (30–79%) | 질환 2개에서 나타남 |
| ZRSR2zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| DNAJC19DnaJ heat shock protein family (Hsp40) member C19 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LSSlanosterol synthase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NONOnon-POU domain containing octamer binding | 가끔 (5–29%) | 질환 1개에서 나타남 |
| RIPK4receptor interacting serine/threonine kinase 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | 기록되지 않음 | 질환 1개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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