Požymis
Narrowing of pulmonic valve
Klinikinis pavadinimas: Pulmonic stenosis
A narrowing of the right ventricular outflow tract that can occur at the pulmonary valve (valvular stenosis), below the pulmonary valve (infundibular stenosis), or above the pulmonary valve (supravalvar stenosis).
Santrauka
- Taip pat vadinama
- Pulmonary stenosis, Pulmonary valve stenosis, Pulmonic valve stenosis
- Kūno sistema
- Abnormality of the cardiovascular system
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/pulmonic-stenosis.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Narrowing of pulmonic valve, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test84 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.
- Noonan SyndromeReads 17 of these genesNRASBRAFHRASKRASMAP2K1MAP2K2About this report →
- Hypertrophic CardiomyopathyReads 17 of these genesNRASBRAFHRASKRASMAP2K1MAP2K2About this report →
- Inherited Congenital Heart DefectsReads 5 of these genesTBX5ELNGATA4GATA6NOTCH1About this report →
- Cornelia de Lange SyndromeReads 3 of these genesRAD21NIPBLSMC3About this report →
Show 80 more reports
- Heterotaxy & Laterality DefectsReads 4 of these genesDAW1ZIC3CIROPGDF1About this report →
- NeurofibromatosisReads 2 of these genesNF1LZTR1About this report →
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- DeSanto-Shinawi SyndromeReads 1 of these genesWACAbout this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- FLT4-Related Congenital Heart DiseaseReads 1 of these genesFLT4About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- Isobutyryl-CoA Dehydrogenase DeficiencyReads 1 of these genesACAD8About this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- Keutel SyndromeReads 1 of these genesMGPAbout this report →
- Lessel-Kreienkamp SyndromeReads 1 of these genesAGO2About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- PLD1-Related Congenital Heart DiseaseReads 1 of these genesPLD1About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Schizophrenia PanelReads 1 of these genesNRXN1About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- SMAD6-Related DisorderReads 1 of these genesSMAD6About this report →
- Snijders Blok-Campeau SyndromeReads 1 of these genesCHD3About this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Marfan Like SyndromesReads 3 of these genesSMAD2FBN1SMAD3About this report →
- Intellectual DisabilityReads 14 of these genesHIVEP2PGAP1ADKCICDDX3XKAT6AAbout this report →
- Mosaic Variegated Aneuploidy SyndromeReads 2 of these genesBUB1BSMC5About this report →
- Adams-Oliver SyndromeReads 2 of these genesNOTCH1ARHGAP31About this report →
- Loeys-Dietz SyndromeReads 2 of these genesSMAD2SMAD3About this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Kabuki SyndromeReads 1 of these genesKDM6AAbout this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesWNT4About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 3 of these genesANKS6NEK8NPHP3About this report →
- Hereditary Arterial CalcificationReads 1 of these genesENPP1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 1 of these genesSMARCA4About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 2 of these genesFAT4FLT4About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCOL3A1B4GALT7About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesTRA2BTBCKAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesKAT6ARAB23About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 2 of these genesSTRA6BCORAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesZNF341About this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- GlaucomaReads 1 of these genesLTBP2About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Inherited ThrombocytopeniasReads 2 of these genesRAP1BCDC42About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesSOX17About this report →
- Polycystic Kidney DiseaseReads 1 of these genesNEK8About this report →
- Coffin-Siris SyndromeReads 1 of these genesSMARCA4About this report →
- Severe Congenital NeutropeniaReads 1 of these genesG6PC3About this report →
- Dilated CardiomyopathyReads 2 of these genesRAF1FKTNAbout this report →
- Hypogonadotropic HypogonadismReads 2 of these genesCHD7PLXND1About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Other Inborn Errors of ImmunityReads 4 of these genesKRASNCF1SKIC3ZNF341About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCUL3About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesGATA4About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesITPR1WASHC5POLR3ATBCKAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesB3GLCTFKTNAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- Congenital Muscular DystrophiesReads 1 of these genesFKTNAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesFKTNAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesPOLR3AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesSKIC3About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesDSG1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesITPR1About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Epilepsy (Full Panel)Reads 2 of these genesSLC6A1ZEB2About this report →
- Primary Ciliary DyskinesiaReads 1 of these genesDAW1About this report →
- Female InfertilityReads 1 of these genesWNT4About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesWASHC5About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
Vienu tyrimu sužinokite genus, susijusius su Narrowing of pulmonic valve, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test148 genų susiję su Narrowing of pulmonic valve
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Narrowing of pulmonic valve. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| ADAMTS19ADAM metallopeptidase with thrombospondin type 1 motif 19 | Visada | 1 ligoje |
| AMOTL1angiomotin like 1 | Visada | 1 ligoje |
| CCT3chaperonin containing TCP1 subunit 3 | Visada | 1 ligoje |
| CILK1ciliogenesis associated kinase 1 | Visada | 1 ligoje |
| COL3A1collagen type III alpha 1 chain | Visada | 1 ligoje |
| DAND5DAN domain BMP antagonist family member 5 | Visada | 1 ligoje |
| GPC3glypican 3 | Visada | 1 ligoje |
| IGFBP7insulin like growth factor binding protein 7 | Visada | 1 ligoje |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Visada | 2 ligose |
| NRASNRAS proto-oncogene, GTPase | Visada | 1 ligoje |
| RNU5B-1RNA, U5B small nuclear 1 | Visada | 1 ligoje |
| RPL27ribosomal protein L27 | Visada | 1 ligoje |
| SMAD2SMAD family member 2 | Visada | 1 ligoje |
| TBX5T-box transcription factor 5 | Visada | 1 ligoje |
| B4GALT7beta-1,4-galactosyltransferase 7 | Labai dažnai (80–99%) | 1 ligoje |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Labai dažnai (80–99%) | 5 ligose |
| HRASHRas proto-oncogene, GTPase | Labai dažnai (80–99%) | 2 ligose |
| KRASKRas proto-oncogene, GTPase | Labai dažnai (80–99%) | 3 ligose |
| MAP2K1mitogen-activated protein kinase kinase 1 | Labai dažnai (80–99%) | 4 ligose |
| MAP2K2mitogen-activated protein kinase kinase 2 | Labai dažnai (80–99%) | 4 ligose |
| NF1neurofibromin 1 | Labai dažnai (80–99%) | 6 ligose |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Labai dažnai (80–99%) | 3 ligose |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Labai dažnai (80–99%) | 2 ligose |
| ADAMTS10ADAM metallopeptidase with thrombospondin type 1 motif 10 | Dažnai (30–79%) | 2 ligose |
| B3GLCTbeta 3-glucosyltransferase | Dažnai (30–79%) | 2 ligose |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Dažnai (30–79%) | 1 ligoje |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Dažnai (30–79%) | 1 ligoje |
| CCDC22CCC complex scaffolding subunit CCDC22 | Dažnai (30–79%) | 1 ligoje |
| CCDC32coiled-coil domain containing 32 | Dažnai (30–79%) | 1 ligoje |
| CHD7chromodomain helicase DNA binding protein 7 | Dažnai (30–79%) | 1 ligoje |
| CLIP2CAP-Gly domain containing linker protein 2 | Dažnai (30–79%) | 1 ligoje |
| CUL3cullin 3 | Dažnai (30–79%) | 1 ligoje |
| DAW1dynein assembly factor with WD repeats 1 | Dažnai (30–79%) | 1 ligoje |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Dažnai (30–79%) | 1 ligoje |
| DPYSL5dihydropyrimidinase like 5 | Dažnai (30–79%) | 1 ligoje |
| DSG1desmoglein 1 | Dažnai (30–79%) | 1 ligoje |
| EIF4Heukaryotic translation initiation factor 4H | Dažnai (30–79%) | 1 ligoje |
| ELNelastin | Dažnai (30–79%) | 3 ligose |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Dažnai (30–79%) | 1 ligoje |
| GTF2Igeneral transcription factor IIi | Dažnai (30–79%) | 1 ligoje |
Rodyti dar 108 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| GTF2IRD1GTF2I repeat domain containing 1 | Dažnai (30–79%) | 1 ligoje |
| GTF2IRD2GTF2I repeat domain containing 2 | Dažnai (30–79%) | 1 ligoje |
| HIVEP2HIVEP zinc finger 2 | Dažnai (30–79%) | 1 ligoje |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Dažnai (30–79%) | 1 ligoje |
| KDM2Blysine demethylase 2B | Dažnai (30–79%) | 1 ligoje |
| KIF20Akinesin family member 20A | Dažnai (30–79%) | 1 ligoje |
| LIMK1LIM domain kinase 1 | Dažnai (30–79%) | 1 ligoje |
| LTBP2latent transforming growth factor beta binding protein 2 | Dažnai (30–79%) | 2 ligose |
| METTL27methyltransferase like 27 | Dažnai (30–79%) | 1 ligoje |
| MLXIPLMLX interacting protein like | Dažnai (30–79%) | 1 ligoje |
| MRASmuscle RAS oncogene homolog | Dažnai (30–79%) | 1 ligoje |
| NCF1neutrophil cytosolic factor 1 | Dažnai (30–79%) | 1 ligoje |
| NEK9NIMA related kinase 9 | Dažnai (30–79%) | 1 ligoje |
| PGAP1post-GPI attachment to proteins inositol deacylase 1 | Dažnai (30–79%) | 1 ligoje |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Dažnai (30–79%) | 2 ligose |
| RAD21RAD21 cohesin complex component | Dažnai (30–79%) | 1 ligoje |
| RFC2replication factor C subunit 2 | Dažnai (30–79%) | 1 ligoje |
| RIT1Ras like without CAAX 1 | Dažnai (30–79%) | 1 ligoje |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Dažnai (30–79%) | 2 ligose |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Dažnai (30–79%) | 1 ligoje |
| SOX17SRY-box transcription factor 17 | Dažnai (30–79%) | 1 ligoje |
| SPRED2sprouty related EVH1 domain containing 2 | Dažnai (30–79%) | 1 ligoje |
| STRA6signaling receptor and transporter of retinol STRA6 | Dažnai (30–79%) | 1 ligoje |
| STX1Asyntaxin 1A | Dažnai (30–79%) | 1 ligoje |
| TBL2transducin beta like 2 | Dažnai (30–79%) | 1 ligoje |
| TMEM270transmembrane protein 270 | Dažnai (30–79%) | 1 ligoje |
| VPS35LVPS35 endosomal protein sorting factor like | Dažnai (30–79%) | 1 ligoje |
| VPS37DVPS37D subunit of ESCRT-I | Dažnai (30–79%) | 1 ligoje |
| WASHC5WASH complex subunit 5 | Dažnai (30–79%) | 2 ligose |
| WNT4Wnt family member 4 | Dažnai (30–79%) | 1 ligoje |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Dažnai (30–79%) | 1 ligoje |
| ZIC3Zic family zinc finger 3 | Dažnai (30–79%) | 1 ligoje |
| ACAD8acyl-CoA dehydrogenase family member 8 | Kartais (5–29%) | 1 ligoje |
| ADAMTS17ADAM metallopeptidase with thrombospondin type 1 motif 17 | Kartais (5–29%) | 1 ligoje |
| ADKadenosine kinase | Kartais (5–29%) | 1 ligoje |
| AGO2argonaute RISC catalytic component 2 | Kartais (5–29%) | 1 ligoje |
| ANKS6ankyrin repeat and sterile alpha motif domain containing 6 | Kartais (5–29%) | 1 ligoje |
| ARPC4actin related protein 2/3 complex subunit 4 | Kartais (5–29%) | 1 ligoje |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Kartais (5–29%) | 1 ligoje |
| CACHD1cache domain containing 1 | Kartais (5–29%) | 1 ligoje |
| CICcapicua transcriptional repressor | Kartais (5–29%) | 1 ligoje |
| CIROPciliated left-right organizer metallopeptidase | Kartais (5–29%) | 1 ligoje |
| DCHS1dachsous cadherin-related 1 | Kartais (5–29%) | 1 ligoje |
| DDX3XDEAD-box helicase 3 X-linked | Kartais (5–29%) | 1 ligoje |
| FAT4FAT atypical cadherin 4 | Kartais (5–29%) | 1 ligoje |
| FBN1fibrillin 1 | Kartais (5–29%) | 2 ligose |
| FBXW11F-box and WD repeat domain containing 11 | Kartais (5–29%) | 1 ligoje |
| FRYLFRY like transcription coactivator | Kartais (5–29%) | 1 ligoje |
| G6PC3glucose-6-phosphatase catalytic subunit 3 | Kartais (5–29%) | 1 ligoje |
| GATA4GATA binding protein 4 | Kartais (5–29%) | 2 ligose |
| GATA6GATA binding protein 6 | Kartais (5–29%) | 2 ligose |
| KAT6Alysine acetyltransferase 6A | Kartais (5–29%) | 1 ligoje |
| KDM6Alysine demethylase 6A | Kartais (5–29%) | 1 ligoje |
| KLHL20kelch like family member 20 | Kartais (5–29%) | 1 ligoje |
| LRP4LDL receptor related protein 4 | Kartais (5–29%) | 1 ligoje |
| LZTR1leucine zipper like post translational regulator 1 | Kartais (5–29%) | 2 ligose |
| NEK8NIMA related kinase 8 | Kartais (5–29%) | 2 ligose |
| NIPBLNIPBL cohesin loading factor | Kartais (5–29%) | 1 ligoje |
| NOTCH1notch receptor 1 | Kartais (5–29%) | 1 ligoje |
| NPHP3nephrocystin 3 | Kartais (5–29%) | 1 ligoje |
| OTUD5OTU deubiquitinase 5 | Kartais (5–29%) | 1 ligoje |
| PLD1phospholipase D1 | Kartais (5–29%) | 1 ligoje |
| PLXND1plexin D1 | Kartais (5–29%) | 2 ligose |
| POLR3ARNA polymerase III subunit A | Kartais (5–29%) | 1 ligoje |
| RAP1BRAP1B, member of RAS oncogene family | Kartais (5–29%) | 1 ligoje |
| RNF135ring finger protein 135 | Kartais (5–29%) | 1 ligoje |
| SARDHsarcosine dehydrogenase | Kartais (5–29%) | 1 ligoje |
| SGO1shugoshin 1 | Kartais (5–29%) | 1 ligoje |
| SKIC3SKI3 subunit of superkiller complex | Kartais (5–29%) | 1 ligoje |
| SLC29A3solute carrier family 29 member 3 | Kartais (5–29%) | 1 ligoje |
| SLC6A1solute carrier family 6 member 1 | Kartais (5–29%) | 1 ligoje |
| SLC6A11solute carrier family 6 member 11 | Kartais (5–29%) | 1 ligoje |
| SMAD3SMAD family member 3 | Kartais (5–29%) | 2 ligose |
| SMAD4SMAD family member 4 | Kartais (5–29%) | 1 ligoje |
| SMAD6SMAD family member 6 | Kartais (5–29%) | 1 ligoje |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Kartais (5–29%) | 1 ligoje |
| SMC3structural maintenance of chromosomes 3 | Kartais (5–29%) | 1 ligoje |
| SMC5structural maintenance of chromosomes 5 | Kartais (5–29%) | 1 ligoje |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Kartais (5–29%) | 1 ligoje |
| TBX2T-box transcription factor 2 | Kartais (5–29%) | 1 ligoje |
| TRA2Btransformer 2 beta homolog | Kartais (5–29%) | 1 ligoje |
| WACWW domain containing adaptor with coiled-coil | Kartais (5–29%) | 1 ligoje |
| ZEB2zinc finger E-box binding homeobox 2 | Kartais (5–29%) | 3 ligose |
| ZNF341zinc finger protein 341 | Kartais (5–29%) | 1 ligoje |
| ZNF699zinc finger protein 699 | Kartais (5–29%) | 1 ligoje |
| BPTFbromodomain PHD finger transcription factor | Retai (1–4 %) | 1 ligoje |
| CHD3chromodomain helicase DNA binding protein 3 | Retai (1–4 %) | 1 ligoje |
| CREBBPCREB binding lysine acetyltransferase | Retai (1–4 %) | 2 ligose |
| EP300EP300 lysine acetyltransferase | Retai (1–4 %) | 1 ligoje |
| KDM6Blysine demethylase 6B | Retai (1–4 %) | 1 ligoje |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Retai (1–4 %) | 1 ligoje |
| SPRED1sprouty related EVH1 domain containing 1 | Retai (1–4 %) | 1 ligoje |
| TBCKTBC1 domain containing kinase | Retai (1–4 %) | 1 ligoje |
| ARHGAP31Rho GTPase activating protein 31 | Neužfiksuota | 1 ligoje |
| BCORBCL6 corepressor | Neužfiksuota | 1 ligoje |
| BMP2bone morphogenetic protein 2 | Neužfiksuota | 1 ligoje |
| CDC42cell division cycle 42 | Neužfiksuota | 1 ligoje |
| CHST3carbohydrate sulfotransferase 3 | Neužfiksuota | 1 ligoje |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Neužfiksuota | 1 ligoje |
| FKTNfukutin | Neužfiksuota | 1 ligoje |
| FLT4fms related receptor tyrosine kinase 4 | Neužfiksuota | 1 ligoje |
| GDF1growth differentiation factor 1 | Neužfiksuota | 2 ligose |
| KANSL1KAT8 regulatory NSL complex subunit 1 | Neužfiksuota | 1 ligoje |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Neužfiksuota | 1 ligoje |
| MGPmatrix Gla protein | Neužfiksuota | 1 ligoje |
| NOTCH2notch receptor 2 | Neužfiksuota | 1 ligoje |
| NRXN1neurexin 1 | Neužfiksuota | 1 ligoje |
| RAB23RAB23, member RAS oncogene family | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.19-9814e911.
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