Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
형질
Recurrent pneumonia
An increased susceptibility to pneumonia as manifested by a history of recurrent episodes of pneumonia.
요약
- 다른 명칭
- Multiple pulmonary infections, Pneumonia, recurrent, Pneumonia, recurrent episodes, Pulmonary infection, Pulmonary infections, pulmonary infections, recurrent, Recurrent pulmonary infections
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
이 페이지의 데이터
페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/recurrent-pneumonia.json"
page <- fromJSON(url)
page$trait$nameRecurrent pneumoniaHP:0006532
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
Recurrent pneumonia과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기80 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.
- Other Inborn Errors of ImmunityReads 58 of these genesADABLNKC3CD247CD3ECD79BAbout this report →
- Severe Combined ImmunodeficiencyReads 14 of these genesADACD247CD3ELATNHEJ1RFXAPAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 7 of these genesNFKB2NFKB1LRBACD19CR2ICOSAbout this report →
- Chronic Granulomatous DiseaseReads 5 of these genesCYBBCYBC1CYBANCF1NCF2About this report →
Show 76 more reports
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 6 of these genesBLNKCD79BBTKIGHMTCF3IGLL1About this report →
- Hyper-IgE SyndromeReads 5 of these genesIL6STSTAT3DOCK8SPINK5ZNF341About this report →
- Primary Ciliary DyskinesiaReads 11 of these genesDRC1ODAD4DNAH11CCDC39CCDC40CLXNAbout this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 2 of these genesIKZF2CD27About this report →
- Cutis LaxaReads 4 of these genesEFEMP2FBLN5LTBP1LTBP4About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
- HyperlysinaemiaReads 1 of these genesAASSAbout this report →
- MEGF10-Related MyopathyReads 1 of these genesMEGF10About this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- MTHFD1 DeficiencyReads 1 of these genesMTHFD1About this report →
- Mucopolysaccharidosis Type II (Hunter Syndrome)Reads 1 of these genesIDSAbout this report →
- Mucopolysaccharidosis Type IVA (Morquio A Syndrome)Reads 1 of these genesGALNSAbout this report →
- Mucopolysaccharidosis-Plus SyndromeReads 1 of these genesVPS33AAbout this report →
- Primary Microcephaly 26 (LMNB1)Reads 1 of these genesLMNB1About this report →
- Prolidase DeficiencyReads 1 of these genesPEPDAbout this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Spondylo-Meta-Epiphyseal Dysplasia, Short Limb-Abnormal Calcification TypeReads 1 of these genesDDR2About this report →
- TrimethylaminuriaReads 1 of these genesFMO3About this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Severe Congenital NeutropeniaReads 3 of these genesCXCR4WASCLPBAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 2 of these genesTGFB1EGFRAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesWDR19WDR35About this report →
- Familial Glucocorticoid DeficiencyReads 2 of these genesMRAPNDC1About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3CDAbout this report →
- Lung CancerReads 1 of these genesEGFRAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL11A2About this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Tubular Aggregate MyopathyReads 1 of these genesSTIM1About this report →
- WHIM SyndromeReads 1 of these genesCXCR4About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Polycystic Kidney DiseaseReads 2 of these genesDZIP1LPKHD1About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesGALNSSMPD1IDSGNPTABAbout this report →
- Inherited ThrombocytopeniasReads 3 of these genesARPC1BSTIM1WASAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesLMNB1About this report →
- Familial Paget Disease of BoneReads 1 of these genesTNFRSF11AAbout this report →
- Epidermolysis BullosaReads 2 of these genesDSTPKP1About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesB3GALT6PLOD1About this report →
- Syndromic CraniosynostosisReads 2 of these genesWDR19WDR35About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
- Surfactant Metabolism DysfunctionReads 1 of these genesSFTPCAbout this report →
- Congenital Disorders of GlycosylationReads 4 of these genesALG12B3GALT6PGM3SLC35C1About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesLRBAAbout this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesLEPAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesPOLA1DOCK11About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 1 of these genesC3About this report →
- Intellectual DisabilityReads 5 of these genesPOLA1RAC1RFX7SMARCA2SETBP1About this report →
- DNA Repair DiseaseReads 2 of these genesERCC6NBNAbout this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesAP3B1About this report →
- LipodystrophyReads 1 of these genesCAVIN1About this report →
- Type I InterferonopathiesReads 1 of these genesPOLA1About this report →
- OsteopetrosisReads 1 of these genesTNFRSF11AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 4 of these genesITPR3SMPD1DSTFBLN5About this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC3About this report →
- Ectodermal DysplasiasReads 1 of these genesIKBKGAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesITPR3FBLN5About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesWDR19About this report →
- Autoimmune DiseaseReads 1 of these genesSTAT3About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesDSTAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesRNU4-2About this report →
- Hearing Loss and DeafnessReads 2 of these genesIKZF2COL11A2About this report →
- VitreoretinopathyReads 1 of these genesIKBKGAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesSERPINH1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesLMNB1RNF168TBCDAbout this report →
- Male InfertilityReads 1 of these genesCFTRAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesLEPAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesRNF168About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesLMNB1About this report →
Recurrent pneumonia과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기연관 유전자 159개: Recurrent pneumonia
이 유전자들의 변화는 Recurrent pneumonia 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 |
|---|---|---|
| ADAadenosine deaminase | 항상 | 질환 2개에서 나타남 |
| ALG12ALG12 alpha-1,6-mannosyltransferase | 항상 | 질환 2개에서 나타남 |
| B3GALT6beta-1,3-galactosyltransferase 6 | 항상 | 질환 1개에서 나타남 |
| BLNKB cell linker | 항상 | 질환 1개에서 나타남 |
| C3complement C3 | 항상 | 질환 1개에서 나타남 |
| CD247CD247 molecule | 항상 | 질환 2개에서 나타남 |
| CD3ECD3 epsilon subunit of T-cell receptor complex | 항상 | 질환 2개에서 나타남 |
| CD79BCD79b molecule | 항상 | 질환 1개에서 나타남 |
| CEBPECCAAT enhancer binding protein epsilon | 항상 | 질환 1개에서 나타남 |
| COPZ1coat protein complex I subunit zeta 1 | 항상 | 질환 1개에서 나타남 |
| CYBBcytochrome b-245 beta chain | 항상 | 질환 1개에서 나타남 |
| CYBC1cytochrome b-245 chaperone 1 | 항상 | 질환 1개에서 나타남 |
| DOT1LDOT1 like histone lysine methyltransferase | 항상 | 질환 1개에서 나타남 |
| DRC1dynein regulatory complex subunit 1 | 항상 | 질환 1개에서 나타남 |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | 항상 | 질환 1개에서 나타남 |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | 항상 | 질환 1개에서 나타남 |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | 항상 | 질환 1개에서 나타남 |
| GALNSgalactosamine (N-acetyl)-6-sulfatase | 항상 | 질환 1개에서 나타남 |
| IGBP1immunoglobulin binding protein 1 | 항상 | 질환 1개에서 나타남 |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | 항상 | 질환 1개에서 나타남 |
| IKZF2IKAROS family zinc finger 2 | 항상 | 질환 2개에서 나타남 |
| IL21Rinterleukin 21 receptor | 항상 | 질환 1개에서 나타남 |
| IL6STinterleukin 6 cytokine family signal transducer | 항상 | 질환 2개에서 나타남 |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | 항상 | 질환 1개에서 나타남 |
| IRF4interferon regulatory factor 4 | 항상 | 질환 1개에서 나타남 |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | 항상 | 질환 1개에서 나타남 |
| LATlinker for activation of T cells | 항상 | 질환 1개에서 나타남 |
| MAN2B2mannosidase alpha class 2B member 2 | 항상 | 질환 1개에서 나타남 |
| MASP2MBL associated serine protease 2 | 항상 | 질환 1개에서 나타남 |
| MEGF10multiple EGF like domains 10 | 항상 | 질환 1개에서 나타남 |
| MOCS3molybdenum cofactor synthesis 3 | 항상 | 질환 1개에서 나타남 |
| MRAPmelanocortin 2 receptor accessory protein | 항상 | 질환 1개에서 나타남 |
| NHEJ1non-homologous end joining factor 1 | 항상 | 질환 1개에서 나타남 |
| NME5NME/NM23 family member 5 | 항상 | 질환 1개에서 나타남 |
| ODAD4outer dynein arm docking complex subunit 4 | 항상 | 질환 1개에서 나타남 |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | 항상 | 질환 1개에서 나타남 |
| PLD4phospholipase D family member 4 | 항상 | 질환 1개에서 나타남 |
| POLA1DNA polymerase alpha 1, catalytic subunit | 항상 | 질환 1개에서 나타남 |
| PTCRApre T cell antigen receptor alpha | 항상 | 질환 1개에서 나타남 |
| RELBRELB proto-oncogene, NF-kB subunit | 항상 | 질환 1개에서 나타남 |
유전자 119개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| RFXAPregulatory factor X associated protein | 항상 | 질환 1개에서 나타남 |
| RNU6ATACRNA, U6atac small nuclear | 항상 | 질환 1개에서 나타남 |
| SERPINH1serpin family H member 1 | 항상 | 질환 1개에서 나타남 |
| SFTPCsurfactant protein C | 항상 | 질환 1개에서 나타남 |
| SMARCD2SWI/SNF related BAF chromatin remodeling complex subunit D2 | 항상 | 질환 1개에서 나타남 |
| STK36serine/threonine kinase 36 | 항상 | 질환 1개에서 나타남 |
| TM2D3TM2 domain containing 3 | 항상 | 질환 1개에서 나타남 |
| TNFRSF13CTNF receptor superfamily member 13C | 항상 | 질환 2개에서 나타남 |
| UNC119unc-119 lipid binding chaperone | 항상 | 질환 1개에서 나타남 |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | 항상 | 질환 1개에서 나타남 |
| BTKBruton tyrosine kinase | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| DNAH11dynein axonemal heavy chain 11 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| NBNnibrin | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| NFKB2nuclear factor kappa B subunit 2 | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| RFX5regulatory factor X5 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| RFXANKregulatory factor X associated ankyrin containing protein | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| STAT3signal transducer and activator of transcription 3 | 매우 자주 (80–99%) | 질환 2개에서 나타남 |
| ALMS1ALMS1 centrosome and basal body associated protein | 자주 (30–79%) | 질환 2개에서 나타남 |
| AP3B1adaptor related protein complex 3 subunit beta 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ARPC1Bactin related protein 2/3 complex subunit 1B | 자주 (30–79%) | 질환 1개에서 나타남 |
| CARMIL2capping protein regulator and myosin 1 linker 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CAVIN1caveolae associated protein 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | 자주 (30–79%) | 질환 1개에서 나타남 |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | 자주 (30–79%) | 질환 1개에서 나타남 |
| CFTRCF transmembrane conductance regulator | 자주 (30–79%) | 질환 1개에서 나타남 |
| CLXNcalaxin | 자주 (30–79%) | 질환 1개에서 나타남 |
| CXCR4C-X-C motif chemokine receptor 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| DOCK2dedicator of cytokinesis 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| DOCK8dedicator of cytokinesis 8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| EXTL3exostosin like glycosyltransferase 3 | 자주 (30–79%) | 질환 2개에서 나타남 |
| FCGR2AFc gamma receptor IIa | 자주 (30–79%) | 질환 1개에서 나타남 |
| IGHMimmunoglobulin heavy constant mu | 자주 (30–79%) | 질환 1개에서 나타남 |
| IL2RGinterleukin 2 receptor subunit gamma | 자주 (30–79%) | 질환 1개에서 나타남 |
| KCNJ6potassium inwardly rectifying channel subfamily J member 6 | 자주 (30–79%) | 질환 2개에서 나타남 |
| LMNB1lamin B1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MED25mediator complex subunit 25 | 자주 (30–79%) | 질환 2개에서 나타남 |
| NFKB1nuclear factor kappa B subunit 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ODAD1outer dynein arm docking complex subunit 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ODAD2outer dynein arm docking complex subunit 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| PGM3phosphoglucomutase 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| RAC2Rac family small GTPase 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| RNF168ring finger protein 168 | 자주 (30–79%) | 질환 1개에서 나타남 |
| RNU4-2RNA, U4 small nuclear 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| RNU4ATACRNA, U4atac small nuclear | 자주 (30–79%) | 질환 2개에서 나타남 |
| SIAH1siah E3 ubiquitin protein ligase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SMPD1sphingomyelin phosphodiesterase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SPINK5serine peptidase inhibitor Kazal type 5 | 자주 (30–79%) | 질환 1개에서 나타남 |
| STIM1stromal interaction molecule 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| STK4serine/threonine kinase 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TBX1T-box transcription factor 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TCF3transcription factor 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TGFB1transforming growth factor beta 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| WASWASP actin nucleation promoting factor | 자주 (30–79%) | 질환 1개에서 나타남 |
| WDR1WD repeat domain 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| WDR19WD repeat domain 19 | 자주 (30–79%) | 질환 1개에서 나타남 |
| WDR35WD repeat domain 35 | 자주 (30–79%) | 질환 1개에서 나타남 |
| AASSaminoadipate-semialdehyde synthase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CD27CD27 molecule | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CD3DCD3 delta subunit of T-cell receptor complex | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CFAP410cilia and flagella associated protein 410 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CLPBClpB family mitochondrial disaggregase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DNAAF4dynein axonemal assembly factor 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DOCK11dedicator of cytokinesis 11 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DSTdystonin | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DZIP1LDAZ interacting zinc finger protein 1 like | 가끔 (5–29%) | 질환 1개에서 나타남 |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FBLN5fibulin 5 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FBXW7F-box and WD repeat domain containing 7 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IGHG2immunoglobulin heavy constant gamma 2 (G2m marker) | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IGKCimmunoglobulin kappa constant | 가끔 (5–29%) | 질환 1개에서 나타남 |
| JAK3Janus kinase 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| KPTNkaptin, actin binding protein | 가끔 (5–29%) | 질환 2개에서 나타남 |
| LRBALPS responsive beige-like anchor protein | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LTBP1latent transforming growth factor beta binding protein 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LTBP4latent transforming growth factor beta binding protein 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NDC1NDC1 transmembrane nucleoporin | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NKX2-1NK2 homeobox 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PKP1plakophilin 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PURApurine rich element binding protein A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| RAC1Rac family small GTPase 1 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| RFX7regulatory factor X7 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| RNF125ring finger protein 125 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SLC35C1solute carrier family 35 member C1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SREBF1sterol regulatory element binding transcription factor 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| STAT5Bsignal transducer and activator of transcription 5B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TONSLtonsoku like, DNA repair protein | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ZBTB7Azinc finger and BTB domain containing 7A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ZNF341zinc finger protein 341 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ZNFX1zinc finger NFX1-type containing 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IDSiduronate 2-sulfatase | 드물게 (1–4%) | 질환 1개에서 나타남 |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | 드물게 (1–4%) | 질환 2개에서 나타남 |
| SETBP1SET binding protein 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| TBCDtubulin folding cofactor D | 드물게 (1–4%) | 질환 1개에서 나타남 |
| CD19CD19 molecule | 기록되지 않음 | 질환 1개에서 나타남 |
| COL11A2collagen type XI alpha 2 chain | 기록되지 않음 | 질환 1개에서 나타남 |
| CR2complement C3d receptor 2 | 기록되지 않음 | 질환 1개에서 나타남 |
| CYBAcytochrome b-245 alpha chain | 기록되지 않음 | 질환 1개에서 나타남 |
| DDR2discoidin domain receptor tyrosine kinase 2 | 기록되지 않음 | 질환 1개에서 나타남 |
| DRC4dynein regulatory complex subunit 4 | 기록되지 않음 | 질환 1개에서 나타남 |
| EGFRepidermal growth factor receptor | 기록되지 않음 | 질환 1개에서 나타남 |
| FMO3flavin containing dimethylaniline monoxygenase 3 | 기록되지 않음 | 질환 1개에서 나타남 |
| FOXN1forkhead box N1 | 기록되지 않음 | 질환 1개에서 나타남 |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | 기록되지 않음 | 질환 1개에서 나타남 |
| HYDINHYDIN axonemal central pair apparatus protein | 기록되지 않음 | 질환 1개에서 나타남 |
| ICOSinducible T cell costimulator | 기록되지 않음 | 질환 2개에서 나타남 |
| IGLL1immunoglobulin lambda like polypeptide 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| LEPleptin | 기록되지 않음 | 질환 1개에서 나타남 |
| MTHFD1methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| NCF1neutrophil cytosolic factor 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| NCF2neutrophil cytosolic factor 2 | 기록되지 않음 | 질환 1개에서 나타남 |
| ORC6origin recognition complex subunit 6 | 기록되지 않음 | 질환 1개에서 나타남 |
| PEPDpeptidase D | 기록되지 않음 | 질환 1개에서 나타남 |
| TNFRSF11ATNF receptor superfamily member 11a | 기록되지 않음 | 질환 1개에서 나타남 |
| TNFRSF13BTNF receptor superfamily member 13B | 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.
하위 형질
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.
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