AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Piirre
Webbed fingers or toes
Kliininen nimi: Syndactyly
Webbing or fusion of the fingers or toes, involving soft parts only or including bone structure. Bony fusions are referred to as "bony" syndactyly if the fusion occurs in a radio-ulnar axis. Fusions of bones of the fingers or toes in a proximo-distal axis are referred to as "symphalangism".
Yhteenveto
- Elimistön järjestelmä
- Abnormality of limbsAbnormality of the musculoskeletal system
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Tämä sivu datana
Lisää sivun osoitteen perään .json tai pyydä application/json-muotoa, niin saat sivun JSON-muodossa.
library(jsonlite)
url <- "https://dantelabs.com/traits/syndactyly.json"
page <- fromJSON(url)
page$trait$nameWebbed fingers or toesHP:0001159
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
Lue Webbed fingers or toes-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test55 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.
- Bardet-Biedl and Alström SyndromesReads 22 of these genesBBS9BBS4ARL6BBIP1BBS1BBS10About this report →
- Joubert Syndrome And Related DisordersReads 12 of these genesCPLANE1FAM149B1KIF7OFD1PDE6DTCTN3About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 5 of these genesCDKN1CHMGA2IGF2PLAG1MAGEL2About this report →
- Syndromic CraniosynostosisReads 7 of these genesWDR35MEGF8RAB23FGFR2FGFR3FGFR1About this report →
Show 51 more reports
- Congenital Dyserythropoietic AnaemiasReads 2 of these genesCDAN1CDIN1About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Intellectual DisabilityReads 15 of these genesCREBBPEP300NAA10NSDHLASXL1KDM6BAbout this report →
- Meckel SyndromeReads 3 of these genesTMEM231MKS1TXNDC15About this report →
- Retinitis PigmentosaReads 8 of these genesFLVCR1OFD1TOPORSARL6BBS2CFAP418About this report →
- Inherited Congenital Heart DefectsReads 3 of these genesFLNANOTCH1TBX5About this report →
- Cornelia de Lange SyndromeReads 2 of these genesNIPBLRAD21About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 5 of these genesFLVCR1TMEM216TMEM231CEP290MKS1About this report →
- Epilepsy (Full Panel)Reads 8 of these genesFLNAZEB2CHD2NEXMIFSCN1ASLC2A1About this report →
- Familial Hemiplegic MigraineReads 1 of these genesSCN1AAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesMKRN3About this report →
- Rothmund-Thomson SyndromeReads 1 of these genesCRIPTAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesNPHP1SDCCAG8About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesSOSTAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR35About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesCEP19About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Inherited ThrombocytopeniasReads 2 of these genesRAP1BHOXA11About this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesTRIM32LMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesFIG4SBF1LMNAAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesVAC14SLC2A1About this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR2About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Hypogonadotropic HypogonadismReads 2 of these genesMAGEL2FGFR1About this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesCDKN1CIGF2About this report →
- Cutis LaxaReads 1 of these genesLTBP1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesFAT4About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Epidermolysis BullosaReads 1 of these genesDSPAbout this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesMTRRAbout this report →
- Autoimmune DiseaseReads 1 of these genesCHRNGAbout this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesCHSY1B3GLCTAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Osteogenesis ImperfectaReads 1 of these genesNBASAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesDSPAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesCACNA1GAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesWASHC5About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesNBASAbout this report →
Lue Webbed fingers or toes-nimiseen tai sen kanssa liittyvät geenit ja muu genomisi yhdellä testillä.
Alkaen 449 $Ilmainen toimitus · Tulokset 6–8 viikossa
Tilaa Genome Test159 geeniä, jotka liittyvät piirteeseen Webbed fingers or toes
Näiden geenien muutokset aiheuttavat harvinaisia sairauksia, joissa Webbed fingers or toes esiintyy. Useimmilla, joilla on tämä piirre, ei ole mitään näistä sairauksista, eikä tämän listan geeni kerro mitään kenenkään omasta genomista.
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| BBS9Bardet-Biedl syndrome 9 | Aina | 2 sairaudessa |
| BCORBCL6 corepressor | Aina | 1 sairaudessa |
| BHLHA9basic helix-loop-helix family member a9 | Aina | 1 sairaudessa |
| CHSY1chondroitin sulfate synthase 1 | Aina | 1 sairaudessa |
| CILK1ciliogenesis associated kinase 1 | Aina | 1 sairaudessa |
| CREBBPCREB binding lysine acetyltransferase | Aina | 2 sairaudessa |
| EP300EP300 lysine acetyltransferase | Aina | 3 sairaudessa |
| ERI1exoribonuclease 1 | Aina | 2 sairaudessa |
| FLNAfilamin A | Aina | 3 sairaudessa |
| FLVCR1FLVCR choline and heme transporter 1 | Aina | 1 sairaudessa |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Aina | 1 sairaudessa |
| IRX5iroquois homeobox 5 | Aina | 1 sairaudessa |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Aina | 1 sairaudessa |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Aina | 2 sairaudessa |
| RIPK4receptor interacting serine/threonine kinase 4 | Aina | 1 sairaudessa |
| SOSTsclerostin | Aina | 1 sairaudessa |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Aina | 1 sairaudessa |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Aina | 1 sairaudessa |
| WDR35WD repeat domain 35 | Aina | 2 sairaudessa |
| LRP4LDL receptor related protein 4 | Hyvin usein (80–99%) | 1 sairaudessa |
| MEGF8multiple EGF like domains 8 | Hyvin usein (80–99%) | 1 sairaudessa |
| RAB23RAB23, member RAS oncogene family | Hyvin usein (80–99%) | 1 sairaudessa |
| ASXL1ASXL transcriptional regulator 1 | Usein (30–79%) | 1 sairaudessa |
| BBS4Bardet-Biedl syndrome 4 | Usein (30–79%) | 2 sairaudessa |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Usein (30–79%) | 1 sairaudessa |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Usein (30–79%) | 1 sairaudessa |
| DCHS1dachsous cadherin-related 1 | Usein (30–79%) | 1 sairaudessa |
| DLX5distal-less homeobox 5 | Usein (30–79%) | 1 sairaudessa |
| DSPdesmoplakin | Usein (30–79%) | 1 sairaudessa |
| FAM149B1family with sequence similarity 149 member B1 | Usein (30–79%) | 1 sairaudessa |
| FAT4FAT atypical cadherin 4 | Usein (30–79%) | 2 sairaudessa |
| FBLN1fibulin 1 | Usein (30–79%) | 1 sairaudessa |
| FGFR2fibroblast growth factor receptor 2 | Usein (30–79%) | 4 sairaudessa |
| FIG4FIG4 phosphoinositide 5-phosphatase | Usein (30–79%) | 1 sairaudessa |
| GLI3GLI family zinc finger 3 | Usein (30–79%) | 4 sairaudessa |
| GRB10growth factor receptor bound protein 10 | Usein (30–79%) | 1 sairaudessa |
| HMGA2high mobility group AT-hook 2 | Usein (30–79%) | 1 sairaudessa |
| IGF2insulin like growth factor 2 | Usein (30–79%) | 3 sairaudessa |
| KIAA0753KIAA0753 | Usein (30–79%) | 1 sairaudessa |
| KIF7kinesin family member 7 | Usein (30–79%) | 1 sairaudessa |
Näytä 119 geeniä lisää
| Geeni | Kuinka usein sitä esiintyy | Sairaudet |
|---|---|---|
| LTBP1latent transforming growth factor beta binding protein 1 | Usein (30–79%) | 1 sairaudessa |
| MAPKAPK5MAPK activated protein kinase 5 | Usein (30–79%) | 1 sairaudessa |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Usein (30–79%) | 1 sairaudessa |
| NIPBLNIPBL cohesin loading factor | Usein (30–79%) | 1 sairaudessa |
| NOTCH1notch receptor 1 | Usein (30–79%) | 1 sairaudessa |
| OFD1OFD1 centriole and centriolar satellite protein | Usein (30–79%) | 2 sairaudessa |
| PDE6Dphosphodiesterase 6D | Usein (30–79%) | 1 sairaudessa |
| PLAG1PLAG1 zinc finger | Usein (30–79%) | 1 sairaudessa |
| PORCNporcupine O-acyltransferase | Usein (30–79%) | 1 sairaudessa |
| RAP1BRAP1B, member of RAS oncogene family | Usein (30–79%) | 1 sairaudessa |
| SLC25A24solute carrier family 25 member 24 | Usein (30–79%) | 1 sairaudessa |
| TCTN3tectonic family member 3 | Usein (30–79%) | 1 sairaudessa |
| TMEM216transmembrane protein 216 | Usein (30–79%) | 1 sairaudessa |
| TMEM231transmembrane protein 231 | Usein (30–79%) | 1 sairaudessa |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Usein (30–79%) | 1 sairaudessa |
| VAC14VAC14 component of PIKFYVE complex | Usein (30–79%) | 1 sairaudessa |
| YY1AP1YY1 associated protein 1 | Usein (30–79%) | 2 sairaudessa |
| ZNF699zinc finger protein 699 | Usein (30–79%) | 1 sairaudessa |
| ARL6ARF like GTPase 6 | Joskus (5–29%) | 2 sairaudessa |
| BBIP1BBSome interacting protein 1 | Joskus (5–29%) | 1 sairaudessa |
| BBS1Bardet-Biedl syndrome 1 | Joskus (5–29%) | 2 sairaudessa |
| BBS10Bardet-Biedl syndrome 10 | Joskus (5–29%) | 1 sairaudessa |
| BBS12Bardet-Biedl syndrome 12 | Joskus (5–29%) | 1 sairaudessa |
| BBS2Bardet-Biedl syndrome 2 | Joskus (5–29%) | 1 sairaudessa |
| BBS5Bardet-Biedl syndrome 5 | Joskus (5–29%) | 2 sairaudessa |
| BBS7Bardet-Biedl syndrome 7 | Joskus (5–29%) | 1 sairaudessa |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Joskus (5–29%) | 1 sairaudessa |
| CDAN1codanin 1 | Joskus (5–29%) | 1 sairaudessa |
| CDIN1CDAN1 interacting nuclease 1 | Joskus (5–29%) | 1 sairaudessa |
| CEP19centrosomal protein 19 | Joskus (5–29%) | 1 sairaudessa |
| CEP290centrosomal protein 290 | Joskus (5–29%) | 1 sairaudessa |
| CEP295centrosomal protein 295 | Joskus (5–29%) | 1 sairaudessa |
| CFAP418cilia and flagella associated protein 418 | Joskus (5–29%) | 1 sairaudessa |
| DLL4delta like canonical Notch ligand 4 | Joskus (5–29%) | 1 sairaudessa |
| DVL3dishevelled segment polarity protein 3 | Joskus (5–29%) | 1 sairaudessa |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Joskus (5–29%) | 1 sairaudessa |
| FGF10fibroblast growth factor 10 | Joskus (5–29%) | 1 sairaudessa |
| FGFR3fibroblast growth factor receptor 3 | Joskus (5–29%) | 1 sairaudessa |
| FILIP1filamin A interacting protein 1 | Joskus (5–29%) | 1 sairaudessa |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Joskus (5–29%) | 1 sairaudessa |
| IFT172intraflagellar transport 172 | Joskus (5–29%) | 1 sairaudessa |
| IFT27intraflagellar transport 27 | Joskus (5–29%) | 1 sairaudessa |
| IFT56intraflagellar transport 56 | Joskus (5–29%) | 1 sairaudessa |
| IFT74intraflagellar transport 74 | Joskus (5–29%) | 1 sairaudessa |
| KDM6Blysine demethylase 6B | Joskus (5–29%) | 1 sairaudessa |
| KICS2KICSTOR subunit 2 | Joskus (5–29%) | 1 sairaudessa |
| LZTFL1leucine zipper transcription factor like 1 | Joskus (5–29%) | 1 sairaudessa |
| MAGEL2MAGE family member L2 | Joskus (5–29%) | 1 sairaudessa |
| MED13Lmediator complex subunit 13L | Joskus (5–29%) | 1 sairaudessa |
| MKKSMKKS centrosomal shuttling protein | Joskus (5–29%) | 3 sairaudessa |
| MKRN3makorin ring finger protein 3 | Joskus (5–29%) | 1 sairaudessa |
| MKS1MKS transition zone complex subunit 1 | Joskus (5–29%) | 2 sairaudessa |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Joskus (5–29%) | 1 sairaudessa |
| NARS1asparaginyl-tRNA synthetase 1 | Joskus (5–29%) | 2 sairaudessa |
| NBASNBAS subunit of NRZ tethering complex | Joskus (5–29%) | 1 sairaudessa |
| NEK1NIMA related kinase 1 | Joskus (5–29%) | 1 sairaudessa |
| NPAP1nuclear pore associated protein 1 | Joskus (5–29%) | 1 sairaudessa |
| NPHP1nephrocystin 1 | Joskus (5–29%) | 1 sairaudessa |
| PHF21APHD finger protein 21A | Joskus (5–29%) | 1 sairaudessa |
| PIBF1progesterone immunomodulatory binding factor 1 | Joskus (5–29%) | 1 sairaudessa |
| POGZpogo transposable element derived with ZNF domain | Joskus (5–29%) | 1 sairaudessa |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Joskus (5–29%) | 1 sairaudessa |
| PTBP1polypyrimidine tract binding protein 1 | Joskus (5–29%) | 1 sairaudessa |
| PWAR1Prader Willi/Angelman region RNA 1 | Joskus (5–29%) | 1 sairaudessa |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Joskus (5–29%) | 1 sairaudessa |
| RAD21RAD21 cohesin complex component | Joskus (5–29%) | 1 sairaudessa |
| REREarginine-glutamic acid dipeptide repeats | Joskus (5–29%) | 1 sairaudessa |
| ROR2ROR family WNT receptor 2 | Joskus (5–29%) | 2 sairaudessa |
| SBF1SET binding factor 1 | Joskus (5–29%) | 1 sairaudessa |
| SCAPERS-phase cyclin A associated protein in the ER | Joskus (5–29%) | 1 sairaudessa |
| SCLT1sodium channel and clathrin linker 1 | Joskus (5–29%) | 1 sairaudessa |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Joskus (5–29%) | 1 sairaudessa |
| SEPTIN9septin 9 | Joskus (5–29%) | 1 sairaudessa |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Joskus (5–29%) | 1 sairaudessa |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Joskus (5–29%) | 1 sairaudessa |
| TBX5T-box transcription factor 5 | Joskus (5–29%) | 1 sairaudessa |
| TGFBR2transforming growth factor beta receptor 2 | Joskus (5–29%) | 1 sairaudessa |
| TP63tumor protein p63 | Joskus (5–29%) | 4 sairaudessa |
| TRA2Btransformer 2 beta homolog | Joskus (5–29%) | 1 sairaudessa |
| TRAF7TNF receptor associated factor 7 | Joskus (5–29%) | 1 sairaudessa |
| TRIM32tripartite motif containing 32 | Joskus (5–29%) | 1 sairaudessa |
| TTC8tetratricopeptide repeat domain 8 | Joskus (5–29%) | 1 sairaudessa |
| TXNDC15thioredoxin domain containing 15 | Joskus (5–29%) | 1 sairaudessa |
| WDPCPWD repeat containing planar cell polarity effector | Joskus (5–29%) | 1 sairaudessa |
| ZEB2zinc finger E-box binding homeobox 2 | Joskus (5–29%) | 2 sairaudessa |
| AP2M1adaptor related protein complex 2 subunit mu 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| CHD2chromodomain helicase DNA binding protein 2 | Harvinainen (1–4 %) | 1 sairaudessa |
| LEMD3LEM domain containing 3 | Harvinainen (1–4 %) | 1 sairaudessa |
| MARK2microtubule affinity regulating kinase 2 | Harvinainen (1–4 %) | 1 sairaudessa |
| NEXMIFneurite extension and migration factor | Harvinainen (1–4 %) | 1 sairaudessa |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| SLC2A1solute carrier family 2 member 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| SLC6A1solute carrier family 6 member 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Harvinainen (1–4 %) | 1 sairaudessa |
| ANKRD11ankyrin repeat domain 11 | Ei kirjattu | 1 sairaudessa |
| B3GLCTbeta 3-glucosyltransferase | Ei kirjattu | 1 sairaudessa |
| BLMBLM RecQ like helicase | Ei kirjattu | 1 sairaudessa |
| CCDC22CCC complex scaffolding subunit CCDC22 | Ei kirjattu | 1 sairaudessa |
| CCDC28Bcoiled-coil domain containing 28B | Ei kirjattu | 1 sairaudessa |
| CHRNGcholinergic receptor nicotinic gamma subunit | Ei kirjattu | 1 sairaudessa |
| CRIPTCXXC repeat containing interactor of PDZ3 domain | Ei kirjattu | 1 sairaudessa |
| DHODHdihydroorotate dehydrogenase (quinone) | Ei kirjattu | 1 sairaudessa |
| DYNC2I1dynein 2 intermediate chain 1 | Ei kirjattu | 1 sairaudessa |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Ei kirjattu | 1 sairaudessa |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Ei kirjattu | 1 sairaudessa |
| FGFR1fibroblast growth factor receptor 1 | Ei kirjattu | 2 sairaudessa |
| HOXA11homeobox A11 | Ei kirjattu | 1 sairaudessa |
| HOXD13homeobox D13 | Ei kirjattu | 1 sairaudessa |
| IFT81intraflagellar transport 81 | Ei kirjattu | 1 sairaudessa |
| LMBR1limb development membrane protein 1 | Ei kirjattu | 1 sairaudessa |
| LMNAlamin A/C | Ei kirjattu | 1 sairaudessa |
| MED12mediator complex subunit 12 | Ei kirjattu | 1 sairaudessa |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Ei kirjattu | 1 sairaudessa |
| PTDSS1phosphatidylserine synthase 1 | Ei kirjattu | 1 sairaudessa |
| SALL4spalt like transcription factor 4 | Ei kirjattu | 1 sairaudessa |
| TWIST1twist family bHLH transcription factor 1 | Ei kirjattu | 1 sairaudessa |
| WASHC5WASH complex subunit 5 | Ei kirjattu | 1 sairaudessa |
| WNT7AWnt family member 7A | Ei kirjattu | 1 sairaudessa |
| ZSWIM6zinc finger SWIM-type containing 6 | Ei kirjattu | 1 sairaudessa |
Kuinka usein ilmiö esiintyy ihmisillä, joilla on jokin geenin sairauksista, niin kuin Human Phenotype Ontology sen kirjaa. Nämä sivut kuvaavat piirteitä ja niiden taustalla olevaa tutkimusta, eivätkä ne ole diagnoosi. Oireista kannattaa kysyä lääkäriltä tai geneettiseltä neuvojalta.
Tarkemmat piirteet
Laajemmat piirteet
Mistä tämä tieto tulee
- Human Phenotype Ontology, julkaisu 2026-09-01: piirre, sen nimet, määritelmä ja siihen liitetyt geenit. Lue lisää osoitteesta hpo.jax.org.
- Tietojulkaisu 2026.10.16-c6eea6bf.
AtlasKeitä autammeTieteemmeTuotteetTulokset
Kirjaudu sisäänKysySekvensoi genomisi↗
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Ilmainen toimitus · Tulokset 6–8 viikossa
