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Tratto
Abnormally close eyes
Nome clinico: Hypotelorism
Interpupillary distance less than 2 SD below the mean (alternatively, the appearance of an decreased interpupillary distance or closely spaced eyes).
Riepilogo
- Detto anche
- Closely spaced eyes, Decreased distance between eye sockets, Decreased distance between eyes, Decreased interpupillary distance, Decreased orbital separation, Ocular hypotelorism
- Sistema corporeo
- Abnormality of the eye
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Aggiunga .json all'indirizzo della pagina, oppure richieda application/json, per leggerla come JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypotelorism.json"
page <- fromJSON(url)
page$trait$nameAbnormally close eyesHP:0000601
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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.
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- Non-Acquired Combined Pituitary Hormone DeficiencyReads 10 of these genesSIX3CDONDISP1GLI2PLCH1PTCH1About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
Show 76 more reports
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- ACBD5 DeficiencyReads 1 of these genesACBD5About this report →
- Alkuraya-Kucinskas SyndromeReads 1 of these genesBLTP1About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- DLL1-Related Neurodevelopmental DisorderReads 1 of these genesDLL1About this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- HyperlysinaemiaReads 1 of these genesAASSAbout this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Phenylketonuria (PKU)Reads 1 of these genesPAHAbout this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- RTTN-Related Microcephalic Primordial DwarfismReads 1 of these genesRTTNAbout this report →
- Scalp-Ear-Nipple SyndromeReads 1 of these genesKCTD1About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- TRAPPC9-Related Intellectual DisabilityReads 1 of these genesTRAPPC9About this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- Intellectual DisabilityReads 14 of these genesKDM6BDYRK1ATRAPPC9CAMK2AHNRNPCHNRNPH2About this report →
- Cornelia de Lange SyndromeReads 2 of these genesSMC1ARAD21About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 4 of these genesSHHRAB3GAP1RAB3GAP2ERCC2About this report →
- Cutis LaxaReads 3 of these genesELNPYCR1ALDH18A1About this report →
- Cantú SyndromeReads 1 of these genesABCC9About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesMSX2About this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Tubular Aggregate MyopathyReads 1 of these genesSTIM1About this report →
- Hypogonadotropic HypogonadismReads 5 of these genesFGFR1FGF8RAB3GAP2SNRPNPROKR2About this report →
- Lissencephaly Spectrum DisordersReads 3 of these genesNDE1RAB3GAP1RAB3GAP2About this report →
- DNA Repair DiseaseReads 4 of these genesGTF2H5ERCC2ERCC3FANCD2About this report →
- Coffin-Siris SyndromeReads 2 of these genesBICRAARID1BAbout this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Rothmund-Thomson SyndromeReads 1 of these genesRECQL4About this report →
- Familial Atrial FibrillationReads 1 of these genesGJA5About this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesGATA2About this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPDE4DAbout this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesCEP57About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesPAN2RNU4-2About this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFRBAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesGATA2About this report →
- Nephrotic SyndromeReads 2 of these genesNUP107NUP133About this report →
- Epilepsy (Full Panel)Reads 5 of these genesRNU2-2SMC1AAARS1CDK19HNRNPH2About this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesPRPS1About this report →
- Inherited ThrombocytopeniasReads 2 of these genesSRCSTIM1About this report →
- Osteogenesis ImperfectaReads 2 of these genesPOLR3APYCR1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesSNRPNAbout this report →
- Joubert Syndrome And Related DisordersReads 2 of these genesSUFUMKS1About this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- Inherited Neurodegenerative DisordersReads 6 of these genesAARS1GPT2POLR3AQARS1ALDH18A1MKS1About this report →
- Congenital Disorders of GlycosylationReads 3 of these genesATP6AP1DPM2SLC35A1About this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesAP3D1About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Other Inborn Errors of ImmunityReads 4 of these genesATP6AP1GATA2LIG4STIM1About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesKIF26AAbout this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesGPT2ALDH18A1About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesSTILAbout this report →
- Fanconi AnemiaReads 1 of these genesFANCD2About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesPRPS1AARS1About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesAARS1POLR3AAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesWDR19About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesFKBP14About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKS1About this report →
- Dyskeratosis CongenitaReads 1 of these genesDCLRE1BAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesPRPS1AARS1SEPTIN9About this report →
- VitreoretinopathyReads 1 of these genesNDPAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesDPM2About this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesLIG4About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJA1About this report →
- Dilated CardiomyopathyReads 1 of these genesABCC9About this report →
- Female InfertilityReads 1 of these genesNUP107About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesMKS1About this report →
- Retinitis PigmentosaReads 1 of these genesIFT43About this report →
- Hearing Loss and DeafnessReads 1 of these genesPRPS1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesPOLRMTAbout this report →
Leggi i geni collegati a Abnormally close eyes e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test157 geni collegati a Abnormally close eyes
Alterazioni in questi geni causano malattie rare in cui si osserva Abnormally close eyes. 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 |
|---|---|---|
| ACBD5acyl-CoA binding domain containing 5 | Sempre | In 1 condizione |
| AP3D1adaptor related protein complex 3 subunit delta 1 | Sempre | In 1 condizione |
| ATP6AP1ATPase H+ transporting accessory protein 1 | Sempre | In 1 condizione |
| CEP57centrosomal protein 57 | Sempre | In 1 condizione |
| CILK1ciliogenesis associated kinase 1 | Sempre | In 1 condizione |
| COX14cytochrome c oxidase assembly factor COX14 | Sempre | In 1 condizione |
| FGFR1fibroblast growth factor receptor 1 | Sempre | In 6 condizioni |
| FKBP14FKBP prolyl isomerase 14 | Sempre | In 1 condizione |
| GTF2H5general transcription factor IIH subunit 5 | Sempre | In 2 condizioni |
| KDM6Alysine demethylase 6A | Sempre | In 1 condizione |
| KDM6Blysine demethylase 6B | Sempre | In 1 condizione |
| KMT2Dlysine methyltransferase 2D | Sempre | In 1 condizione |
| NINninein | Sempre | In 2 condizioni |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Sempre | In 1 condizione |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Sempre | In 1 condizione |
| RNU2-2RNA, U2 small nuclear 2 | Sempre | In 1 condizione |
| SIX3SIX homeobox 3 | Sempre | In 6 condizioni |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Sempre | In 1 condizione |
| XRCC4X-ray repair cross complementing 4 | Sempre | In 1 condizione |
| CDONcell adhesion associated, oncogene regulated | Molto spesso (80–99%) | In 6 condizioni |
| CRIPTOcripto, EGF-CFC family member | Molto spesso (80–99%) | In 5 condizioni |
| DISP1dispatched RND transporter family member 1 | Molto spesso (80–99%) | In 5 condizioni |
| DLL1delta like canonical Notch ligand 1 | Molto spesso (80–99%) | In 5 condizioni |
| FGF8fibroblast growth factor 8 | Molto spesso (80–99%) | In 5 condizioni |
| FOXH1forkhead box H1 | Molto spesso (80–99%) | In 5 condizioni |
| GAS1growth arrest specific 1 | Molto spesso (80–99%) | In 5 condizioni |
| GLI2GLI family zinc finger 2 | Molto spesso (80–99%) | In 7 condizioni |
| NDPnorrin cystine knot growth factor NDP | Molto spesso (80–99%) | In 1 condizione |
| NODALnodal growth differentiation factor | Molto spesso (80–99%) | In 5 condizioni |
| PLCH1phospholipase C eta 1 | Molto spesso (80–99%) | In 1 condizione |
| PTCH1patched 1 | Molto spesso (80–99%) | In 6 condizioni |
| SHHsonic hedgehog signaling molecule | Molto spesso (80–99%) | In 7 condizioni |
| SMC1Astructural maintenance of chromosomes 1A | Molto spesso (80–99%) | In 2 condizioni |
| STAG2STAG2 cohesin complex component | Molto spesso (80–99%) | In 2 condizioni |
| STILSTIL centriolar assembly protein | Molto spesso (80–99%) | In 4 condizioni |
| TGIF1TGFB induced factor homeobox 1 | Molto spesso (80–99%) | In 6 condizioni |
| ZIC2Zic family zinc finger 2 | Molto spesso (80–99%) | In 6 condizioni |
| AARS1alanyl-tRNA synthetase 1 | Spesso (30–79%) | In 2 condizioni |
| ABCC9ATP binding cassette subfamily C member 9 | Spesso (30–79%) | In 1 condizione |
| ARCN1archain 1 coat protein complex I subunit delta | Spesso (30–79%) | In 1 condizione |
Mostra altri 117 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| CCDC32coiled-coil domain containing 32 | Spesso (30–79%) | In 1 condizione |
| CDK19cyclin dependent kinase 19 | Spesso (30–79%) | In 1 condizione |
| DCLRE1BDNA cross-link repair 1B | Spesso (30–79%) | In 1 condizione |
| DPYSL5dihydropyrimidinase like 5 | Spesso (30–79%) | In 1 condizione |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Spesso (30–79%) | In 1 condizione |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Spesso (30–79%) | In 1 condizione |
| FREM1FRAS1 related extracellular matrix 1 | Spesso (30–79%) | In 1 condizione |
| GGT1gamma-glutamyltransferase 1 | Spesso (30–79%) | In 1 condizione |
| GJA1gap junction protein alpha 1 | Spesso (30–79%) | In 1 condizione |
| GPT2glutamic--pyruvic transaminase 2 | Spesso (30–79%) | In 2 condizioni |
| IFT122intraflagellar transport 122 | Spesso (30–79%) | In 2 condizioni |
| IFT43intraflagellar transport 43 | Spesso (30–79%) | In 1 condizione |
| IFT52intraflagellar transport 52 | Spesso (30–79%) | In 1 condizione |
| LRRC8Cleucine rich repeat containing 8 VRAC subunit C | Spesso (30–79%) | In 1 condizione |
| MSTO1misato mitochondrial distribution and morphology regulator 1 | Spesso (30–79%) | In 1 condizione |
| NDE1nudE neurodevelopment protein 1 | Spesso (30–79%) | In 1 condizione |
| PDGFRBplatelet derived growth factor receptor beta | Spesso (30–79%) | In 1 condizione |
| PI4K2Aphosphatidylinositol 4-kinase type 2 alpha | Spesso (30–79%) | In 1 condizione |
| POLR3ARNA polymerase III subunit A | Spesso (30–79%) | In 1 condizione |
| QARS1glutaminyl-tRNA synthetase 1 | Spesso (30–79%) | In 1 condizione |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Spesso (30–79%) | In 1 condizione |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Spesso (30–79%) | In 1 condizione |
| RAD21RAD21 cohesin complex component | Spesso (30–79%) | In 1 condizione |
| SHPKsedoheptulokinase | Spesso (30–79%) | In 1 condizione |
| SLC4A10solute carrier family 4 member 10 | Spesso (30–79%) | In 1 condizione |
| SUFUSUFU negative regulator of hedgehog signaling | Spesso (30–79%) | In 1 condizione |
| TRAPPC9trafficking protein particle complex subunit 9 | 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 |
| WDR83OSWD repeat domain 83 opposite strand | Spesso (30–79%) | In 1 condizione |
| AASSaminoadipate-semialdehyde synthase | A volte (5–29%) | In 1 condizione |
| BICRABRD4 interacting chromatin remodeling complex associated protein | A volte (5–29%) | In 1 condizione |
| CAMK2Acalcium/calmodulin dependent protein kinase II alpha | A volte (5–29%) | In 1 condizione |
| CAPRIN1cell cycle associated protein 1 | A volte (5–29%) | In 1 condizione |
| CARS1cysteinyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| CLCN3Cl-/H+ antiporter 3 | A volte (5–29%) | In 1 condizione |
| CNOT1CCR4-NOT transcription complex subunit 1 | A volte (5–29%) | In 1 condizione |
| CNOT3CCR4-NOT transcription complex subunit 3 | A volte (5–29%) | In 1 condizione |
| CUX1cut like homeobox 1 | A volte (5–29%) | In 1 condizione |
| DBR1debranching RNA lariats 1 | A volte (5–29%) | In 1 condizione |
| DDB1damage specific DNA binding protein 1 | A volte (5–29%) | In 1 condizione |
| DPM2dolichyl-phosphate mannosyltransferase subunit 2, regulatory | A volte (5–29%) | In 2 condizioni |
| ELNelastin | A volte (5–29%) | In 1 condizione |
| EPG5ectopic P-granules 5 autophagy tethering factor | A volte (5–29%) | In 2 condizioni |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | A volte (5–29%) | In 1 condizione |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | A volte (5–29%) | In 1 condizione |
| FANCD2FA complementation group D2 | A volte (5–29%) | In 1 condizione |
| FGFR2fibroblast growth factor receptor 2 | A volte (5–29%) | In 1 condizione |
| FGFR3fibroblast growth factor receptor 3 | A volte (5–29%) | In 1 condizione |
| GATA2GATA binding protein 2 | A volte (5–29%) | In 1 condizione |
| GNB2G protein subunit beta 2 | A volte (5–29%) | In 1 condizione |
| GON7GON7 subunit of KEOPS complex | A volte (5–29%) | In 1 condizione |
| GTF2E2general transcription factor IIE subunit 2 | A volte (5–29%) | In 1 condizione |
| HNRNPCheterogeneous nuclear ribonucleoprotein C | A volte (5–29%) | In 1 condizione |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | A volte (5–29%) | In 1 condizione |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | A volte (5–29%) | In 1 condizione |
| KANSL1KAT8 regulatory NSL complex subunit 1 | A volte (5–29%) | In 1 condizione |
| KAT8lysine acetyltransferase 8 | A volte (5–29%) | In 1 condizione |
| KCTD1potassium channel tetramerization domain containing 1 | A volte (5–29%) | In 1 condizione |
| KDM2Blysine demethylase 2B | A volte (5–29%) | In 1 condizione |
| KIF26Akinesin family member 26A | A volte (5–29%) | In 1 condizione |
| LAGE3L antigen family member 3 | A volte (5–29%) | In 1 condizione |
| MED16mediator complex subunit 16 | A volte (5–29%) | In 1 condizione |
| MLXIPLMLX interacting protein like | A volte (5–29%) | In 1 condizione |
| MPLKIPM-phase specific PLK1 interacting protein | A volte (5–29%) | In 1 condizione |
| MSL2MSL complex subunit 2 | A volte (5–29%) | In 1 condizione |
| MSX2msh homeobox 2 | A volte (5–29%) | In 1 condizione |
| NF1neurofibromin 1 | A volte (5–29%) | In 1 condizione |
| NTNG2netrin G2 | A volte (5–29%) | In 1 condizione |
| NUP107nucleoporin 107 | A volte (5–29%) | In 1 condizione |
| NUP133nucleoporin 133 | A volte (5–29%) | In 1 condizione |
| OSGEPO-sialoglycoprotein endopeptidase | A volte (5–29%) | In 1 condizione |
| PDE4Dphosphodiesterase 4D | A volte (5–29%) | In 1 condizione |
| POLRMTRNA polymerase mitochondrial | A volte (5–29%) | In 1 condizione |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | A volte (5–29%) | In 2 condizioni |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | A volte (5–29%) | In 1 condizione |
| PYCR1pyrroline-5-carboxylate reductase 1 | A volte (5–29%) | In 1 condizione |
| RECQL4RecQ like helicase 4 | A volte (5–29%) | In 1 condizione |
| REREarginine-glutamic acid dipeptide repeats | A volte (5–29%) | In 1 condizione |
| RNF113Aring finger protein 113A | A volte (5–29%) | In 1 condizione |
| RNU4-2RNA, U4 small nuclear 2 | A volte (5–29%) | In 1 condizione |
| RTTNrotatin | A volte (5–29%) | In 1 condizione |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | A volte (5–29%) | In 1 condizione |
| TARS1threonyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| TP53RKTP53 regulating kinase | A volte (5–29%) | In 1 condizione |
| TPRKBTP53RK binding protein | A volte (5–29%) | In 1 condizione |
| TRMT10AtRNA methyltransferase 10A | A volte (5–29%) | In 1 condizione |
| TWIST1twist family bHLH transcription factor 1 | A volte (5–29%) | In 1 condizione |
| WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit | A volte (5–29%) | In 1 condizione |
| WDR73WD repeat domain 73 | A volte (5–29%) | In 1 condizione |
| YRDCyrdC N6-threonylcarbamoyltransferase domain containing | A volte (5–29%) | In 1 condizione |
| ZNF699zinc finger protein 699 | A volte (5–29%) | In 1 condizione |
| CTCFCCCTC-binding factor | Raramente (1–4%) | In 1 condizione |
| EBF3EBF transcription factor 3 | Raramente (1–4%) | In 1 condizione |
| GJA5gap junction protein alpha 5 | Raramente (1–4%) | In 1 condizione |
| GJA8gap junction protein alpha 8 | Raramente (1–4%) | In 1 condizione |
| NARS1asparaginyl-tRNA synthetase 1 | Raramente (1–4%) | In 1 condizione |
| PAHphenylalanine hydroxylase | Raramente (1–4%) | In 1 condizione |
| SMPD4sphingomyelin phosphodiesterase 4 | Raramente (1–4%) | In 1 condizione |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Non registrato | In 1 condizione |
| ARID1BAT-rich interaction domain 1B | Non registrato | In 1 condizione |
| BLTP1bridge-like lipid transfer protein family member 1 | Non registrato | In 1 condizione |
| EVCEvC ciliary complex subunit 1 | Non registrato | In 1 condizione |
| EVC2EvC ciliary complex subunit 2 | Non registrato | In 1 condizione |
| GSCgoosecoid homeobox | Non registrato | In 1 condizione |
| LIG4DNA ligase 4 | Non registrato | In 1 condizione |
| MKS1MKS transition zone complex subunit 1 | Non registrato | In 1 condizione |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Non registrato | In 1 condizione |
| OPHN1oligophrenin 1 | Non registrato | In 1 condizione |
| PROKR2prokineticin receptor 2 | Non registrato | In 1 condizione |
| RLIMring finger protein, LIM domain interacting | Non registrato | In 1 condizione |
| SEPTIN9septin 9 | Non registrato | In 1 condizione |
| SLC35A1solute carrier family 35 member A1 | Non registrato | In 1 condizione |
| SRCSRC proto-oncogene, non-receptor tyrosine kinase | Non registrato | In 1 condizione |
| STIM1stromal interaction molecule 1 | Non registrato | In 1 condizione |
| TRRAPtransformation/transcription domain associated protein | Non registrato | In 1 condizione |
| USP9Xubiquitin specific peptidase 9 X-linked | 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 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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