Tratto
Long fingers
The middle finger is more than 2 SD above the mean for newborns 27 to 41 weeks EGA or above the 97th centile for children from birth to 16 years of age AND the five digits retain their normal length proportions relative to each other (i.e., it is not the case that the middle finger is the only lengthened digit), or, Fingers that appear disproportionately long compared to the palm of the hand.
Riepilogo
- Sistema corporeo
- Abnormality of limbsAbnormality of the musculoskeletal system
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Ottieni il mio Genome Test50 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.
- Lamb-Shaffer SyndromeReads 1 of these genesSOX5About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Nizon-Isidor SyndromeReads 1 of these genesMED12LAbout this report →
Show 46 more reports
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- TMEM94-Related Intellectual Disability with Heart DefectsReads 1 of these genesTMEM94About this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- Congenital MyopathiesReads 4 of these genesBIN1RYR1SPEGTTNAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Intellectual DisabilityReads 9 of these genesCNKSR2NSDHLGATAD2BRUSC2SMARCA2NAA10About this report →
- Myofibrillar MyopathiesReads 2 of these genesRYR1TTNAbout this report →
- Osteogenesis ImperfectaReads 3 of these genesCOL1A2POLR3AXYLT2About this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesGATA2About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- TubulinopathiesReads 1 of these genesTUBBAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCOL1A2COL3A1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPMM2ALG12COG7ALG3About this report →
- VitreoretinopathyReads 2 of these genesXYLT2COL11A1About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesGATA2About this report →
- Epilepsy (Full Panel)Reads 5 of these genesCNKSR2RNU2-2SPTAN1FLNAGABRA3About this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPHGDHAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesCOL6A2TTNAbout this report →
- Autism Spectrum DisorderReads 1 of these genesTBR1About this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- HyperinsulinismReads 1 of these genesPMM2About this report →
- Type I InterferonopathiesReads 1 of these genesPSMB8About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBBAbout this report →
- Cutis LaxaReads 1 of these genesEFEMP2About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Distal MyopathiesReads 1 of these genesTTNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesSPTAN1SLC12A6About this report →
- Syndromic CraniosynostosisReads 1 of these genesTWIST1About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesSPTAN1About this report →
- Congenital Muscular DystrophiesReads 1 of these genesCOL6A2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPSMB8About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesNR4A2About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesSPTAN1POLR3ASLC12A6About this report →
- Male InfertilityReads 1 of these genesBCORL1About this report →
- Dilated CardiomyopathyReads 1 of these genesTTNAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesSPTAN1SLC12A6About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesSPTAN1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesCOL11A1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesGATA2About this report →
Leggi i geni collegati a Long fingers e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test72 geni collegati a Long fingers
Alterazioni in questi geni causano malattie rare in cui si osserva Long fingers. 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 |
|---|---|---|
| AMOTL1angiomotin like 1 | Sempre | In 1 condizione |
| ATXN7L3ataxin 7 like 3 | Sempre | In 1 condizione |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | Sempre | In 1 condizione |
| CRNKL1crooked neck pre-mRNA splicing factor 1 | Sempre | In 1 condizione |
| DHRS3dehydrogenase/reductase 3 | Sempre | In 1 condizione |
| EBPEBP cholestenol delta-isomerase | Sempre | In 2 condizioni |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Sempre | In 1 condizione |
| FBN1fibrillin 1 | Sempre | In 2 condizioni |
| GON4Lgon-4 like | Sempre | In 1 condizione |
| PAPPA2pappalysin 2 | Sempre | In 1 condizione |
| RNU2-2RNA, U2 small nuclear 2 | Sempre | In 1 condizione |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Sempre | In 1 condizione |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Sempre | In 1 condizione |
| FLNAfilamin A | Molto spesso (80–99%) | In 1 condizione |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Molto spesso (80–99%) | In 1 condizione |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Molto spesso (80–99%) | In 1 condizione |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Molto spesso (80–99%) | In 1 condizione |
| TBR1T-box brain transcription factor 1 | Molto spesso (80–99%) | In 1 condizione |
| TBX4T-box transcription factor 4 | Molto spesso (80–99%) | In 1 condizione |
| ADAMTSL1ADAMTS like 1 | Spesso (30–79%) | In 1 condizione |
| BCORL1BCL6 corepressor like 1 | Spesso (30–79%) | In 1 condizione |
| COL1A2collagen type I alpha 2 chain | Spesso (30–79%) | In 1 condizione |
| DOCK3dedicator of cytokinesis 3 | Spesso (30–79%) | In 1 condizione |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Spesso (30–79%) | In 1 condizione |
| GATAD2BGATA zinc finger domain containing 2B | Spesso (30–79%) | In 2 condizioni |
| NFIXnuclear factor I X | Spesso (30–79%) | In 2 condizioni |
| NPR3natriuretic peptide receptor 3 | Spesso (30–79%) | In 1 condizione |
| PHGDHphosphoglycerate dehydrogenase | Spesso (30–79%) | In 1 condizione |
| PLAAphospholipase A2 activating protein | Spesso (30–79%) | In 2 condizioni |
| PMM2phosphomannomutase 2 | Spesso (30–79%) | In 1 condizione |
| POLR3ARNA polymerase III subunit A | Spesso (30–79%) | In 2 condizioni |
| PTRH2peptidyl-tRNA hydrolase 2 | Spesso (30–79%) | In 2 condizioni |
| RUSC2RUN and SH3 domain containing 2 | Spesso (30–79%) | In 1 condizione |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Spesso (30–79%) | In 1 condizione |
| TMCO1transmembrane and coiled-coil domains 1 | Spesso (30–79%) | In 1 condizione |
| TMEM94transmembrane protein 94 | Spesso (30–79%) | In 1 condizione |
| TPRtranslocated promoter region, nuclear basket protein | Spesso (30–79%) | In 1 condizione |
| TWIST1twist family bHLH transcription factor 1 | Spesso (30–79%) | In 1 condizione |
| WLSWnt ligand secretion mediator | Spesso (30–79%) | In 1 condizione |
| XYLT2xylosyltransferase 2 | Spesso (30–79%) | In 1 condizione |
Mostra altri 32 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ALG12ALG12 alpha-1,6-mannosyltransferase | A volte (5–29%) | In 1 condizione |
| BIN1bridging integrator 1 | A volte (5–29%) | In 1 condizione |
| BORCS8BLOC-1 related complex subunit 8 | A volte (5–29%) | In 1 condizione |
| CLCN3Cl-/H+ antiporter 3 | A volte (5–29%) | In 1 condizione |
| COG7component of oligomeric golgi complex 7 | A volte (5–29%) | In 1 condizione |
| COL6A2collagen type VI alpha 2 chain | A volte (5–29%) | In 1 condizione |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | A volte (5–29%) | In 1 condizione |
| GATA2GATA binding protein 2 | A volte (5–29%) | In 1 condizione |
| H4C5H4 clustered histone 5 | A volte (5–29%) | In 1 condizione |
| LARS1leucyl-tRNA synthetase 1 | A volte (5–29%) | In 1 condizione |
| MAPRE2microtubule associated protein RP/EB family member 2 | A volte (5–29%) | In 1 condizione |
| MED12Lmediator complex subunit 12L | A volte (5–29%) | In 1 condizione |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | A volte (5–29%) | In 1 condizione |
| PUF60poly(U) binding splicing factor 60 | A volte (5–29%) | In 1 condizione |
| RFX7regulatory factor X7 | A volte (5–29%) | In 1 condizione |
| RYR1ryanodine receptor 1 | A volte (5–29%) | In 1 condizione |
| SOX5SRY-box transcription factor 5 | A volte (5–29%) | In 1 condizione |
| SPEGstriated muscle enriched protein kinase | A volte (5–29%) | In 1 condizione |
| TTNtitin | A volte (5–29%) | In 1 condizione |
| TUBBtubulin beta class I | A volte (5–29%) | In 1 condizione |
| YY1YY1 transcription factor | A volte (5–29%) | In 1 condizione |
| ALG3ALG3 alpha-1,3- mannosyltransferase | Non registrato | In 1 condizione |
| COL11A1collagen type XI alpha 1 chain | Non registrato | In 1 condizione |
| COL3A1collagen type III alpha 1 chain | Non registrato | In 1 condizione |
| CPT2carnitine palmitoyltransferase 2 | Non registrato | In 1 condizione |
| EEDembryonic ectoderm development | Non registrato | In 1 condizione |
| IRX5iroquois homeobox 5 | Non registrato | In 1 condizione |
| PCGF2polycomb group ring finger 2 | Non registrato | In 1 condizione |
| PSMB8proteasome 20S subunit beta 8 | Non registrato | In 1 condizione |
| SLC12A6solute carrier family 12 member 6 | Non registrato | In 1 condizione |
| SMSspermine synthase | Non registrato | In 1 condizione |
| ZMIZ1zinc finger MIZ-type containing 1 | 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.
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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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