Atlas이런 분들을 위해과학적 근거제품연구 성과
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형질
Hypergonadotropic hypogonadism
Reduced function of the gonads (testes in males or ovaries in females) associated with excess pituitary gonadotropin secretion and resulting in delayed sexual development and growth delay.
요약
- 다른 명칭
- Hypergonadotrophic hypogonadism, Primary hypogonadism
Atlas이런 분들을 위해과학적 근거제품연구 성과
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페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypergonadotropic-hypogonadism.json"
page <- fromJSON(url)
page$trait$nameHypergonadotropic hypogonadismHP:0000815
Atlas이런 분들을 위해과학적 근거제품연구 성과
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Hypergonadotropic hypogonadism과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
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내 Genome Test 받기61 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.
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 9 of these genesDHHSRYDHX37GATA4MAP3K1NR5A1About this report →
- Fanconi AnemiaReads 5 of these genesFANCD2FANCAFANCBFANCCFANCEAbout this report →
- Female InfertilityReads 8 of these genesBMP15NUP107CYP19A1NR5A1FOXL2CLPPAbout this report →
- DNA Repair DiseaseReads 7 of these genesMRE11FANCD2APTXFANCAFANCBFANCCAbout this report →
Show 57 more reports
- 46,XX Differences of Sex DevelopmentReads 2 of these genesSRYNR5A1About this report →
- GalactosemiaReads 2 of these genesGALK1GALTAbout this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- POLR1C-Related DisorderReads 1 of these genesPOLR1CAbout this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- POLR3B-Related DisorderReads 1 of these genesPOLR3BAbout this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Hypertrophic CardiomyopathyReads 6 of these genesDHHSRYDHX37MAP3K1NR5A1ZFPM2About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 2 of these genesLEPRLEPAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Primary Mitochondrial DiseaseReads 8 of these genesPRORPLIG3POLGRRM2BTYMPMGME1About this report →
- Inherited Neurodegenerative DisordersReads 13 of these genesSCP2SQSTM1POLR1CPOLR3APOLR3BSIL1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 3 of these genesPOLR1CPOLR3APOLR3BAbout this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- Monogenic Precocious PubertyReads 1 of these genesLHCGRAbout this report →
- Myelodysplastic Syndrome (MDS)Reads 1 of these genesSAMD9About this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Hypogonadotropic HypogonadismReads 4 of these genesLEPRLEPNR0B1DCAF17About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesSIL1WWOXCTDP1TWNKAbout this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesSAMD9About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Treacher Collins SyndromeReads 1 of these genesPOLR1CAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesLMNAPOLR3BLIG3POLGRRM2BTYMPAbout this report →
- Other Inherited LeukodystrophiesReads 4 of these genesSCP2POLR1CPOLR3APOLR3BAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesCYB5AAbout this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesAMACRAbout this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesCYP17A1About this report →
- Diabetes MellitusReads 2 of these genesGATA4ZBTB20About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesDCAF17About this report →
- HyperinsulinismReads 1 of these genesPMM2About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Type I InterferonopathiesReads 1 of these genesPOLA1About this report →
- Frontotemporal DementiaReads 1 of these genesSQSTM1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Cutis LaxaReads 1 of these genesRIN2About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesLSSAbout this report →
- Amelogenesis ImperfectaReads 1 of these genesITGB6About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesLMNAPOLR3BAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesLSSAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesSQSTM1About this report →
- Nephrotic SyndromeReads 1 of these genesNUP107About this report →
- Thyroid CancerReads 1 of these genesGNASAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPOLA1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesDCAF17About this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPMM2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesWWOXAbout this report →
- Intellectual DisabilityReads 1 of these genesPOLA1About this report →
Hypergonadotropic hypogonadism과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기연관 유전자 64개: Hypergonadotropic hypogonadism
이 유전자들의 변화는 Hypergonadotropic hypogonadism 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 |
|---|---|---|
| BMP15bone morphogenetic protein 15 | 항상 | 질환 1개에서 나타남 |
| BMPR1Bbone morphogenetic protein receptor type 1B | 항상 | 질환 1개에서 나타남 |
| DHHdesert hedgehog signaling molecule | 항상 | 질환 1개에서 나타남 |
| LEPRleptin receptor | 항상 | 질환 2개에서 나타남 |
| NUP107nucleoporin 107 | 항상 | 질환 1개에서 나타남 |
| SCP2sterol carrier protein 2 | 항상 | 질환 1개에서 나타남 |
| SQSTM1sequestosome 1 | 항상 | 질환 1개에서 나타남 |
| SRYsex determining region Y | 항상 | 질환 2개에서 나타남 |
| CYB5Acytochrome b5 type A | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| CYP19A1cytochrome P450 family 19 subfamily A member 1 | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| DHX37DEAH-box helicase 37 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| GATA4GATA binding protein 4 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| LEPleptin | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| LMNAlamin A/C | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| NR0B1nuclear receptor subfamily 0 group B member 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| NR5A1nuclear receptor subfamily 5 group A member 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| POLA1DNA polymerase alpha 1, catalytic subunit | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| POLR1CRNA polymerase I and III subunit C | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| POLR3ARNA polymerase III subunit A | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| POLR3BRNA polymerase III subunit B | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| SIL1SIL1 nucleotide exchange factor | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| SOX9SRY-box transcription factor 9 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| VAMP7vesicle associated membrane protein 7 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| WT1WT1 transcription factor | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| WWOXWW domain containing oxidoreductase | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| ZFPM2zinc finger protein, FOG family member 2 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| AHSGalpha 2-HS glycoprotein | 자주 (30–79%) | 질환 1개에서 나타남 |
| ALMS1ALMS1 centrosome and basal body associated protein | 자주 (30–79%) | 질환 2개에서 나타남 |
| BRCC3BRCA1/BRCA2-containing complex subunit 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ITGB6integrin subunit beta 6 | 자주 (30–79%) | 질환 1개에서 나타남 |
| LSSlanosterol synthase | 자주 (30–79%) | 질환 1개에서 나타남 |
| MANFmesencephalic astrocyte derived neurotrophic factor | 자주 (30–79%) | 질환 1개에서 나타남 |
| MRPS7mitochondrial ribosomal protein S7 | 자주 (30–79%) | 질환 1개에서 나타남 |
| PRORPprotein only RNase P catalytic subunit | 자주 (30–79%) | 질환 1개에서 나타남 |
| FOXL2forkhead box L2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GALK1galactokinase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GNASGNAS complex locus | 가끔 (5–29%) | 질환 2개에서 나타남 |
| LIG3DNA ligase 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
유전자 24개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| MRE11MRE11 double strand break repair nuclease | 가끔 (5–29%) | 질환 1개에서 나타남 |
| POLGDNA polymerase gamma, catalytic subunit | 가끔 (5–29%) | 질환 2개에서 나타남 |
| RIN2Ras and Rab interactor 2 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SAMD9sterile alpha motif domain containing 9 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TYMPthymidine phosphorylase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ZBTB20zinc finger and BTB domain containing 20 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FANCD2FA complementation group D2 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| MGME1mitochondrial genome maintenance exonuclease 1 | 드물게 (1–4%) | 질환 2개에서 나타남 |
| AMACRalpha-methylacyl-CoA racemase | 기록되지 않음 | 질환 1개에서 나타남 |
| APTXaprataxin | 기록되지 않음 | 질환 1개에서 나타남 |
| CLPPcaseinolytic mitochondrial matrix peptidase proteolytic subunit | 기록되지 않음 | 질환 1개에서 나타남 |
| COQ2coenzyme Q2, polyprenyltransferase | 기록되지 않음 | 질환 1개에서 나타남 |
| CTDP1CTD phosphatase 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| DCAF17DDB1 and CUL4 associated factor 17 | 기록되지 않음 | 질환 1개에서 나타남 |
| FANCAFA complementation group A | 기록되지 않음 | 질환 1개에서 나타남 |
| FANCBFA complementation group B | 기록되지 않음 | 질환 1개에서 나타남 |
| FANCCFA complementation group C | 기록되지 않음 | 질환 1개에서 나타남 |
| FANCEFA complementation group E | 기록되지 않음 | 질환 1개에서 나타남 |
| GALTgalactose-1-phosphate uridylyltransferase | 기록되지 않음 | 질환 1개에서 나타남 |
| LHCGRluteinizing hormone/choriogonadotropin receptor | 기록되지 않음 | 질환 1개에서 나타남 |
| PMM2phosphomannomutase 2 | 기록되지 않음 | 질환 1개에서 나타남 |
| SLC29A3solute carrier family 29 member 3 | 기록되지 않음 | 질환 1개에서 나타남 |
| TWNKtwinkle mtDNA helicase | 기록되지 않음 | 질환 2개에서 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.
Atlas이런 분들을 위해과학적 근거제품연구 성과
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