Tratto
Clubbing of fingers and toes
Nome clinico: Clubbing
Broadening of the soft tissues (non-edematous swelling of soft tissues) of the digital tips in all dimensions associated with an increased longitudinal and lateral curvature of the nails.
Riepilogo
- Detto anche
- Digital clubbing
- Sistema corporeo
- Abnormality of limbsAbnormality of the musculoskeletal system
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page$trait$nameLeggi i geni collegati a Clubbing of fingers and toes e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test37 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.
- Primary Ciliary DyskinesiaReads 46 of these genesCCDC39CCDC40CCNOCFAP221CFAP298CFAP300About this report →
- Surfactant Metabolism DysfunctionReads 4 of these genesSFTPCMARS1ABCA3SFTPBAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 3 of these genesSMAD4ACVRL1ENGAbout this report →
- Juvenile Polyposis SyndromeReads 2 of these genesSMAD4BMPR1AAbout this report →
Show 33 more reports
- CHAPLE Disease (CD55 Deficiency)Reads 1 of these genesCD55About this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- Mucopolysaccharidosis-Plus SyndromeReads 1 of these genesVPS33AAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- Peutz-Jeghers SyndromeReads 1 of these genesSTK11About this report →
- Stüve-Wiedemann SyndromeReads 1 of these genesLIFRAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 3 of these genesSCNN1ASCNN1BSCNN1GAbout this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 1 of these genesFLNBAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Familial Pulmonary FibrosisReads 2 of these genesPOT1SFTPA1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 3 of these genesKRT1KRT16KRT9About this report →
- MelanomaReads 1 of these genesPOT1About this report →
- DNA Repair DiseaseReads 3 of these genesERCC2ERCC3GTF2H5About this report →
- Male InfertilityReads 3 of these genesDNAH1SPEF2CFTRAbout this report →
- Inherited IchthyosesReads 2 of these genesKRT1ABCA12About this report →
- Hyper-IgE SyndromeReads 1 of these genesIL6STAbout this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesDAW1About this report →
- Type I InterferonopathiesReads 1 of these genesPOLA1About this report →
- Intellectual DisabilityReads 4 of these genesSMAD4POLA1TCF4ZFXAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesAARS1MARS1About this report →
- Retinitis PigmentosaReads 2 of these genesOFD1RPGRAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesPOT1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZFXAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesIL6STMALT1IRF1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesERCC2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPOLA1About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesOFD1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesAARS1MARS1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesAARS1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesAARS1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesAARS1About this report →
Leggi i geni collegati a Clubbing of fingers and toes e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test103 geni collegati a Clubbing of fingers and toes
Alterazioni in questi geni causano malattie rare in cui si osserva Clubbing of fingers and toes. 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 |
|---|---|---|
| DONSONDNA replication fork stabilization factor DONSON | Sempre | In 1 condizione |
| HPGD15-hydroxyprostaglandin dehydrogenase | Sempre | In 3 condizioni |
| IL6STinterleukin 6 cytokine family signal transducer | Sempre | In 1 condizione |
| MALT1MALT1 paracaspase | Sempre | In 1 condizione |
| POT1protection of telomeres 1 | Sempre | In 1 condizione |
| VPS51VPS51 subunit of GARP complex | Sempre | In 1 condizione |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Molto spesso (80–99%) | In 2 condizioni |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Spesso (30–79%) | In 1 condizione |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Spesso (30–79%) | In 2 condizioni |
| IRF1interferon regulatory factor 1 | Spesso (30–79%) | In 1 condizione |
| KRT1keratin 1 | Spesso (30–79%) | In 1 condizione |
| KRT16keratin 16 | Spesso (30–79%) | In 1 condizione |
| KRT9keratin 9 | Spesso (30–79%) | In 1 condizione |
| LIFRLIF receptor subunit alpha | Spesso (30–79%) | In 1 condizione |
| RNF31ring finger protein 31 | Spesso (30–79%) | In 1 condizione |
| SFTPA1surfactant protein A1 | Spesso (30–79%) | In 1 condizione |
| SFTPCsurfactant protein C | Spesso (30–79%) | In 1 condizione |
| SMAD4SMAD family member 4 | Spesso (30–79%) | In 2 condizioni |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Spesso (30–79%) | In 1 condizione |
| AARS1alanyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| ABCA12ATP binding cassette subfamily A member 12 | A volte (5–29%) | In 1 condizione |
| BMPR1Abone morphogenetic protein receptor type 1A | A volte (5–29%) | In 1 condizione |
| BRWD1bromodomain and WD repeat domain containing 1 | A volte (5–29%) | In 1 condizione |
| CARS1cysteinyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| CCDC39coiled-coil domain 39 molecular ruler complex subunit | A volte (5–29%) | In 1 condizione |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | A volte (5–29%) | In 1 condizione |
| CCNOcyclin O | A volte (5–29%) | In 1 condizione |
| CDC45cell division cycle 45 | A volte (5–29%) | In 1 condizione |
| CFAP221cilia and flagella associated protein 221 | A volte (5–29%) | In 1 condizione |
| CFAP298cilia and flagella associated protein 298 | A volte (5–29%) | In 1 condizione |
| CFAP300cilia and flagella associated protein 300 | A volte (5–29%) | In 1 condizione |
| CFAP74cilia and flagella associated protein 74 | A volte (5–29%) | In 1 condizione |
| CLXNcalaxin | A volte (5–29%) | In 1 condizione |
| DAW1dynein assembly factor with WD repeats 1 | A volte (5–29%) | In 1 condizione |
| DBR1debranching RNA lariats 1 | A volte (5–29%) | In 1 condizione |
| DNAAF1dynein axonemal assembly factor 1 | A volte (5–29%) | In 1 condizione |
| DNAAF11dynein axonemal assembly factor 11 | A volte (5–29%) | In 1 condizione |
| DNAAF19dynein axonemal assembly factor 19 | A volte (5–29%) | In 1 condizione |
| DNAAF2dynein axonemal assembly factor 2 | A volte (5–29%) | In 1 condizione |
| DNAAF3dynein axonemal assembly factor 3 | A volte (5–29%) | In 1 condizione |
Mostra altri 63 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| DNAAF4dynein axonemal assembly factor 4 | A volte (5–29%) | In 1 condizione |
| DNAAF5dynein axonemal assembly factor 5 | A volte (5–29%) | In 1 condizione |
| DNAAF6dynein axonemal assembly factor 6 | A volte (5–29%) | In 1 condizione |
| DNAH1dynein axonemal heavy chain 1 | A volte (5–29%) | In 1 condizione |
| DNAH11dynein axonemal heavy chain 11 | A volte (5–29%) | In 1 condizione |
| DNAH5dynein axonemal heavy chain 5 | A volte (5–29%) | In 1 condizione |
| DNAH7dynein axonemal heavy chain 7 | A volte (5–29%) | In 1 condizione |
| DNAH9dynein axonemal heavy chain 9 | A volte (5–29%) | In 1 condizione |
| DNAI1dynein axonemal intermediate chain 1 | A volte (5–29%) | In 1 condizione |
| DNAI2dynein axonemal intermediate chain 2 | A volte (5–29%) | In 1 condizione |
| DNAJB13DnaJ heat shock protein family (Hsp40) member B13 | A volte (5–29%) | In 1 condizione |
| DNAL1dynein axonemal light chain 1 | A volte (5–29%) | In 1 condizione |
| DRC1dynein regulatory complex subunit 1 | A volte (5–29%) | In 1 condizione |
| DRC2dynein regulatory complex subunit 2 | A volte (5–29%) | In 1 condizione |
| DRC4dynein regulatory complex subunit 4 | A volte (5–29%) | In 1 condizione |
| 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 |
| FOXJ1forkhead box J1 | A volte (5–29%) | In 1 condizione |
| GAS2L2growth arrest specific 2 like 2 | A volte (5–29%) | In 1 condizione |
| GTF2E2general transcription factor IIE subunit 2 | A volte (5–29%) | In 1 condizione |
| GTF2H5general transcription factor IIH subunit 5 | A volte (5–29%) | In 1 condizione |
| HYDINHYDIN axonemal central pair apparatus protein | A volte (5–29%) | In 1 condizione |
| LRRC56leucine rich repeat containing 56 | A volte (5–29%) | In 1 condizione |
| MARS1methionyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| MCIDASmulticiliate differentiation and DNA synthesis associated cell cycle protein | A volte (5–29%) | In 1 condizione |
| MPLKIPM-phase specific PLK1 interacting protein | A volte (5–29%) | In 1 condizione |
| NEK10NIMA related kinase 10 | A volte (5–29%) | In 1 condizione |
| NME5NME/NM23 family member 5 | A volte (5–29%) | In 1 condizione |
| NME8NME/NM23 family member 8 | A volte (5–29%) | In 1 condizione |
| ODAD1outer dynein arm docking complex subunit 1 | A volte (5–29%) | In 1 condizione |
| ODAD2outer dynein arm docking complex subunit 2 | A volte (5–29%) | In 1 condizione |
| ODAD3outer dynein arm docking complex subunit 3 | A volte (5–29%) | In 1 condizione |
| ODAD4outer dynein arm docking complex subunit 4 | A volte (5–29%) | In 1 condizione |
| OFD1OFD1 centriole and centriolar satellite protein | A volte (5–29%) | In 1 condizione |
| POLA1DNA polymerase alpha 1, catalytic subunit | A volte (5–29%) | In 1 condizione |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | A volte (5–29%) | In 1 condizione |
| RNF113Aring finger protein 113A | A volte (5–29%) | In 1 condizione |
| RPGRretinitis pigmentosa GTPase regulator | A volte (5–29%) | In 1 condizione |
| RSPH1radial spoke head component 1 | A volte (5–29%) | In 1 condizione |
| RSPH3radial spoke head 3 | A volte (5–29%) | In 1 condizione |
| RSPH4Aradial spoke head component 4A | A volte (5–29%) | In 1 condizione |
| RSPH9radial spoke head component 9 | A volte (5–29%) | In 1 condizione |
| SPAG1sperm associated antigen 1 | A volte (5–29%) | In 1 condizione |
| SPEF2sperm flagellar and cilia associated 2 | A volte (5–29%) | In 1 condizione |
| STK36serine/threonine kinase 36 | A volte (5–29%) | In 1 condizione |
| TARS1threonyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| TCF4transcription factor 4 | A volte (5–29%) | In 1 condizione |
| TTC12tetratricopeptide repeat domain 12 | A volte (5–29%) | In 1 condizione |
| ZFXzinc finger protein X-linked | A volte (5–29%) | In 1 condizione |
| ZMYND10zinc finger MYND-type containing 10 | A volte (5–29%) | In 1 condizione |
| CFTRCF transmembrane conductance regulator | Raramente (1–4%) | In 1 condizione |
| SCNN1Asodium channel epithelial 1 subunit alpha | Raramente (1–4%) | In 1 condizione |
| SCNN1Bsodium channel epithelial 1 subunit beta | Raramente (1–4%) | In 1 condizione |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Raramente (1–4%) | In 1 condizione |
| ABCA3ATP binding cassette subfamily A member 3 | Non registrato | In 1 condizione |
| ACVRL1activin A receptor like type 1 | Non registrato | In 1 condizione |
| BTNL2butyrophilin like 2 | Non registrato | In 1 condizione |
| CD55CD55 molecule (Cromer blood group) | Non registrato | In 1 condizione |
| ENGendoglin | Non registrato | In 1 condizione |
| FLNBfilamin B | Non registrato | In 1 condizione |
| SFTPBsurfactant protein B | Non registrato | In 1 condizione |
| SMARCAD1SNF2 related chromatin remodeling ATPase with DExD box 1 | Non registrato | In 1 condizione |
| STK11serine/threonine kinase 11 | 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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