Tratto
Recurrent pneumonia
An increased susceptibility to pneumonia as manifested by a history of recurrent episodes of pneumonia.
Riepilogo
- Detto anche
- Multiple pulmonary infections, Pneumonia, recurrent, Pneumonia, recurrent episodes, Pulmonary infection, Pulmonary infections, pulmonary infections, recurrent, Recurrent pulmonary infections
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page$trait$nameLeggi i geni collegati a Recurrent pneumonia e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test80 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 →
Leggi i geni collegati a Recurrent pneumonia e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test159 geni collegati a Recurrent pneumonia
Alterazioni in questi geni causano malattie rare in cui si osserva Recurrent pneumonia. 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 |
|---|---|---|
| ADAadenosine deaminase | Sempre | In 2 condizioni |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Sempre | In 2 condizioni |
| B3GALT6beta-1,3-galactosyltransferase 6 | Sempre | In 1 condizione |
| BLNKB cell linker | Sempre | In 1 condizione |
| C3complement C3 | Sempre | In 1 condizione |
| CD247CD247 molecule | Sempre | In 2 condizioni |
| CD3ECD3 epsilon subunit of T-cell receptor complex | Sempre | In 2 condizioni |
| CD79BCD79b molecule | Sempre | In 1 condizione |
| CEBPECCAAT enhancer binding protein epsilon | Sempre | In 1 condizione |
| COPZ1coat protein complex I subunit zeta 1 | Sempre | In 1 condizione |
| CYBBcytochrome b-245 beta chain | Sempre | In 1 condizione |
| CYBC1cytochrome b-245 chaperone 1 | Sempre | In 1 condizione |
| DOT1LDOT1 like histone lysine methyltransferase | Sempre | In 1 condizione |
| DRC1dynein regulatory complex subunit 1 | Sempre | In 1 condizione |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Sempre | In 1 condizione |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | Sempre | In 1 condizione |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Sempre | In 1 condizione |
| GALNSgalactosamine (N-acetyl)-6-sulfatase | Sempre | In 1 condizione |
| IGBP1immunoglobulin binding protein 1 | Sempre | In 1 condizione |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Sempre | In 1 condizione |
| IKZF2IKAROS family zinc finger 2 | Sempre | In 2 condizioni |
| IL21Rinterleukin 21 receptor | Sempre | In 1 condizione |
| IL6STinterleukin 6 cytokine family signal transducer | Sempre | In 2 condizioni |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Sempre | In 1 condizione |
| IRF4interferon regulatory factor 4 | Sempre | In 1 condizione |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Sempre | In 1 condizione |
| LATlinker for activation of T cells | Sempre | In 1 condizione |
| MAN2B2mannosidase alpha class 2B member 2 | Sempre | In 1 condizione |
| MASP2MBL associated serine protease 2 | Sempre | In 1 condizione |
| MEGF10multiple EGF like domains 10 | Sempre | In 1 condizione |
| MOCS3molybdenum cofactor synthesis 3 | Sempre | In 1 condizione |
| MRAPmelanocortin 2 receptor accessory protein | Sempre | In 1 condizione |
| NHEJ1non-homologous end joining factor 1 | Sempre | In 1 condizione |
| NME5NME/NM23 family member 5 | Sempre | In 1 condizione |
| ODAD4outer dynein arm docking complex subunit 4 | Sempre | In 1 condizione |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sempre | In 1 condizione |
| PLD4phospholipase D family member 4 | Sempre | In 1 condizione |
| POLA1DNA polymerase alpha 1, catalytic subunit | Sempre | In 1 condizione |
| PTCRApre T cell antigen receptor alpha | Sempre | In 1 condizione |
| RELBRELB proto-oncogene, NF-kB subunit | Sempre | In 1 condizione |
Mostra altri 119 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| RFXAPregulatory factor X associated protein | Sempre | In 1 condizione |
| RNU6ATACRNA, U6atac small nuclear | Sempre | In 1 condizione |
| SERPINH1serpin family H member 1 | Sempre | In 1 condizione |
| SFTPCsurfactant protein C | Sempre | In 1 condizione |
| SMARCD2SWI/SNF related BAF chromatin remodeling complex subunit D2 | Sempre | In 1 condizione |
| STK36serine/threonine kinase 36 | Sempre | In 1 condizione |
| TM2D3TM2 domain containing 3 | Sempre | In 1 condizione |
| TNFRSF13CTNF receptor superfamily member 13C | Sempre | In 2 condizioni |
| UNC119unc-119 lipid binding chaperone | Sempre | In 1 condizione |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Sempre | In 1 condizione |
| BTKBruton tyrosine kinase | Molto spesso (80–99%) | In 2 condizioni |
| DNAH11dynein axonemal heavy chain 11 | Molto spesso (80–99%) | In 1 condizione |
| NBNnibrin | Molto spesso (80–99%) | In 2 condizioni |
| NFKB2nuclear factor kappa B subunit 2 | Molto spesso (80–99%) | In 2 condizioni |
| RFX5regulatory factor X5 | Molto spesso (80–99%) | In 1 condizione |
| RFXANKregulatory factor X associated ankyrin containing protein | Molto spesso (80–99%) | In 1 condizione |
| STAT3signal transducer and activator of transcription 3 | Molto spesso (80–99%) | In 2 condizioni |
| ALMS1ALMS1 centrosome and basal body associated protein | Spesso (30–79%) | In 2 condizioni |
| AP3B1adaptor related protein complex 3 subunit beta 1 | Spesso (30–79%) | In 1 condizione |
| ARPC1Bactin related protein 2/3 complex subunit 1B | Spesso (30–79%) | In 1 condizione |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Spesso (30–79%) | In 1 condizione |
| CAVIN1caveolae associated protein 1 | Spesso (30–79%) | In 1 condizione |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | Spesso (30–79%) | In 1 condizione |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Spesso (30–79%) | In 1 condizione |
| CFTRCF transmembrane conductance regulator | Spesso (30–79%) | In 1 condizione |
| CLXNcalaxin | Spesso (30–79%) | In 1 condizione |
| CXCR4C-X-C motif chemokine receptor 4 | Spesso (30–79%) | In 1 condizione |
| DOCK2dedicator of cytokinesis 2 | Spesso (30–79%) | In 1 condizione |
| DOCK8dedicator of cytokinesis 8 | Spesso (30–79%) | In 1 condizione |
| EXTL3exostosin like glycosyltransferase 3 | Spesso (30–79%) | In 2 condizioni |
| FCGR2AFc gamma receptor IIa | Spesso (30–79%) | In 1 condizione |
| IGHMimmunoglobulin heavy constant mu | Spesso (30–79%) | In 1 condizione |
| IL2RGinterleukin 2 receptor subunit gamma | Spesso (30–79%) | In 1 condizione |
| KCNJ6potassium inwardly rectifying channel subfamily J member 6 | Spesso (30–79%) | In 2 condizioni |
| LMNB1lamin B1 | Spesso (30–79%) | In 1 condizione |
| MED25mediator complex subunit 25 | Spesso (30–79%) | In 2 condizioni |
| NFKB1nuclear factor kappa B subunit 1 | Spesso (30–79%) | In 1 condizione |
| ODAD1outer dynein arm docking complex subunit 1 | Spesso (30–79%) | In 1 condizione |
| ODAD2outer dynein arm docking complex subunit 2 | Spesso (30–79%) | In 1 condizione |
| PGM3phosphoglucomutase 3 | Spesso (30–79%) | In 1 condizione |
| RAC2Rac family small GTPase 2 | Spesso (30–79%) | In 1 condizione |
| RNF168ring finger protein 168 | Spesso (30–79%) | In 1 condizione |
| RNU4-2RNA, U4 small nuclear 2 | Spesso (30–79%) | In 1 condizione |
| RNU4ATACRNA, U4atac small nuclear | Spesso (30–79%) | In 2 condizioni |
| SIAH1siah E3 ubiquitin protein ligase 1 | Spesso (30–79%) | In 1 condizione |
| SMPD1sphingomyelin phosphodiesterase 1 | Spesso (30–79%) | In 1 condizione |
| SPINK5serine peptidase inhibitor Kazal type 5 | Spesso (30–79%) | In 1 condizione |
| STIM1stromal interaction molecule 1 | Spesso (30–79%) | In 1 condizione |
| STK4serine/threonine kinase 4 | Spesso (30–79%) | In 1 condizione |
| TBX1T-box transcription factor 1 | Spesso (30–79%) | In 1 condizione |
| TCF3transcription factor 3 | Spesso (30–79%) | In 1 condizione |
| TGFB1transforming growth factor beta 1 | Spesso (30–79%) | In 1 condizione |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Spesso (30–79%) | In 1 condizione |
| WASWASP actin nucleation promoting factor | Spesso (30–79%) | In 1 condizione |
| WDR1WD repeat domain 1 | Spesso (30–79%) | In 1 condizione |
| WDR19WD repeat domain 19 | Spesso (30–79%) | In 1 condizione |
| WDR35WD repeat domain 35 | Spesso (30–79%) | In 1 condizione |
| AASSaminoadipate-semialdehyde synthase | A volte (5–29%) | In 1 condizione |
| CD27CD27 molecule | A volte (5–29%) | In 1 condizione |
| CD3DCD3 delta subunit of T-cell receptor complex | A volte (5–29%) | In 1 condizione |
| CFAP410cilia and flagella associated protein 410 | A volte (5–29%) | In 1 condizione |
| CLPBClpB family mitochondrial disaggregase | A volte (5–29%) | In 1 condizione |
| DNAAF4dynein axonemal assembly factor 4 | A volte (5–29%) | In 1 condizione |
| DOCK11dedicator of cytokinesis 11 | A volte (5–29%) | In 1 condizione |
| DSTdystonin | A volte (5–29%) | In 1 condizione |
| DZIP1LDAZ interacting zinc finger protein 1 like | A volte (5–29%) | In 1 condizione |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | A volte (5–29%) | In 1 condizione |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | A volte (5–29%) | In 1 condizione |
| FBLN5fibulin 5 | A volte (5–29%) | In 1 condizione |
| FBXW7F-box and WD repeat domain containing 7 | A volte (5–29%) | In 1 condizione |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | A volte (5–29%) | In 1 condizione |
| IGHG2immunoglobulin heavy constant gamma 2 (G2m marker) | A volte (5–29%) | In 1 condizione |
| IGKCimmunoglobulin kappa constant | A volte (5–29%) | In 1 condizione |
| JAK3Janus kinase 3 | A volte (5–29%) | In 1 condizione |
| KPTNkaptin, actin binding protein | A volte (5–29%) | In 2 condizioni |
| LRBALPS responsive beige-like anchor protein | A volte (5–29%) | In 1 condizione |
| LTBP1latent transforming growth factor beta binding protein 1 | A volte (5–29%) | In 1 condizione |
| LTBP4latent transforming growth factor beta binding protein 4 | A volte (5–29%) | In 1 condizione |
| NDC1NDC1 transmembrane nucleoporin | A volte (5–29%) | In 1 condizione |
| NKX2-1NK2 homeobox 1 | A volte (5–29%) | In 1 condizione |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | A volte (5–29%) | In 1 condizione |
| PKP1plakophilin 1 | A volte (5–29%) | In 1 condizione |
| PURApurine rich element binding protein A | A volte (5–29%) | In 1 condizione |
| RAC1Rac family small GTPase 1 | A volte (5–29%) | In 2 condizioni |
| RFX7regulatory factor X7 | A volte (5–29%) | In 1 condizione |
| RNF125ring finger protein 125 | A volte (5–29%) | In 1 condizione |
| SLC35C1solute carrier family 35 member C1 | A volte (5–29%) | In 1 condizione |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | A volte (5–29%) | In 1 condizione |
| SREBF1sterol regulatory element binding transcription factor 1 | A volte (5–29%) | In 1 condizione |
| STAT5Bsignal transducer and activator of transcription 5B | A volte (5–29%) | In 1 condizione |
| TONSLtonsoku like, DNA repair protein | A volte (5–29%) | In 1 condizione |
| ZBTB7Azinc finger and BTB domain containing 7A | A volte (5–29%) | In 1 condizione |
| ZNF341zinc finger protein 341 | A volte (5–29%) | In 1 condizione |
| ZNFX1zinc finger NFX1-type containing 1 | A volte (5–29%) | In 1 condizione |
| IDSiduronate 2-sulfatase | Raramente (1–4%) | In 1 condizione |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Raramente (1–4%) | In 2 condizioni |
| SETBP1SET binding protein 1 | Raramente (1–4%) | In 1 condizione |
| TBCDtubulin folding cofactor D | Raramente (1–4%) | In 1 condizione |
| CD19CD19 molecule | Non registrato | In 1 condizione |
| COL11A2collagen type XI alpha 2 chain | Non registrato | In 1 condizione |
| CR2complement C3d receptor 2 | Non registrato | In 1 condizione |
| CYBAcytochrome b-245 alpha chain | Non registrato | In 1 condizione |
| DDR2discoidin domain receptor tyrosine kinase 2 | Non registrato | In 1 condizione |
| DRC4dynein regulatory complex subunit 4 | Non registrato | In 1 condizione |
| EGFRepidermal growth factor receptor | Non registrato | In 1 condizione |
| FMO3flavin containing dimethylaniline monoxygenase 3 | Non registrato | In 1 condizione |
| FOXN1forkhead box N1 | Non registrato | In 1 condizione |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Non registrato | In 1 condizione |
| HYDINHYDIN axonemal central pair apparatus protein | Non registrato | In 1 condizione |
| ICOSinducible T cell costimulator | Non registrato | In 2 condizioni |
| IGLL1immunoglobulin lambda like polypeptide 1 | Non registrato | In 1 condizione |
| LEPleptin | Non registrato | In 1 condizione |
| MTHFD1methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 | Non registrato | In 1 condizione |
| NCF1neutrophil cytosolic factor 1 | Non registrato | In 1 condizione |
| NCF2neutrophil cytosolic factor 2 | Non registrato | In 1 condizione |
| ORC6origin recognition complex subunit 6 | Non registrato | In 1 condizione |
| PEPDpeptidase D | Non registrato | In 1 condizione |
| TNFRSF11ATNF receptor superfamily member 11a | Non registrato | In 1 condizione |
| TNFRSF13BTNF receptor superfamily member 13B | 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 specifici
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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