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Egenskap
Short attention span
Reduced attention span characterized by distractibility and impulsivity.
Sammanfattning
- Även kallad
- Poor attention span, Problem paying attention, Easily distracted, Easy distractibility, High distractibility
- Kroppssystem
- Abnormality of the nervous system
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library(jsonlite)
url <- "https://dantelabs.com/traits/short-attention-span.json"
page <- fromJSON(url)
page$trait$nameShort attention spanHP:0000736
AtlasVem vi hjälperVår vetenskapProdukterResultat
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Läs generna kopplade till Short attention span, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test82 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 genesARL6BBIP1BBS1BBS10BBS12BBS2About this report →
- Parkinson DiseaseReads 10 of these genesATP13A2DNAJC6LRRK2PARK7PINK1PLA2G6About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 8 of these genesCDONDISP1GLI2PTCH1SHHSIX3About this report →
- Intellectual DisabilityReads 22 of these genesCC2D1ACHD8CNKSR2KDM6BPRMT7FOXP1About this report →
Show 78 more reports
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Shwachman-Diamond SyndromeReads 2 of these genesEFL1SBDSAbout this report →
- Hereditary Optic NeuropathyReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- 3-Methylglutaconic Aciduria Type 1Reads 1 of these genesAUHAbout this report →
- 3-Methylglutaconic Aciduria Type 8 (HTRA2)Reads 1 of these genesHTRA2About this report →
- Angelman SyndromeReads 1 of these genesUBE3AAbout this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
- DLL1-Related Neurodevelopmental DisorderReads 1 of these genesDLL1About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- FOXP2-Related Speech and Language DisorderReads 1 of these genesFOXP2About this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- HyperlysinaemiaReads 1 of these genesAASSAbout this report →
- Hyperprolinaemia Type 2Reads 1 of these genesALDH4A1About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Wiedemann-Steiner SyndromeReads 1 of these genesKMT2AAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- X-Linked Opitz G/BBB SyndromeReads 1 of these genesMID1About this report →
- Inherited Neurodegenerative DisordersReads 19 of these genesARSAATP13A2CEP290MKS1MT-ND1MT-ND4About this report →
- Rare Hereditary Peripheral NeuropathiesReads 14 of these genesARSAMT-ND1MT-ND4MT-ND5MT-ND6PSAPAbout this report →
- Epilepsy (Full Panel)Reads 12 of these genesCNKSR2PAK3GABRA1GABRG2GRIN2APCDH19About this report →
- Malignant Endocrine NeoplasmReads 2 of these genesCDKN1BMEN1About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Myotonic DystrophyReads 1 of these genesDMPKAbout this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesPTCH1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 5 of these genesCEP290MKS1SYNE1CYP27A1PNKPAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesATP13A2PLA2G6About this report →
- Hereditary Spastic ParaplegiaReads 5 of these genesATP13A2SPG11ABCD1NIPA1UCHL1About this report →
- Leigh SyndromeReads 5 of these genesMT-ND1MT-ND4MT-ND5MT-ND6SUCLG1About this report →
- Familial Hemiplegic MigraineReads 1 of these genesSCN1AAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesSECISBP2About this report →
- Retinitis PigmentosaReads 5 of these genesARL6BBS2CFAP418IFT172TTC8About this report →
- Lysosomal Storage DiseaseReads 4 of these genesARSAMAN2B1PSAPCYP27A1About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesTUBB3TUBG1About this report →
- Hereditary Episodic AtaxiasReads 1 of these genesSCN2AAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- TubulinopathiesReads 1 of these genesTUBB3About this report →
- Joubert Syndrome And Related DisordersReads 3 of these genesCEP290MKS1NPHP1About this report →
- Other Inherited LeukodystrophiesReads 4 of these genesARSAPSAPABCD1CYP27A1About this report →
- Congenital HypothyroidismReads 2 of these genesSECISBP2NKX2-1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesNPHP1SDCCAG8About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesNTRK1SCN9AAbout this report →
- Noonan SyndromeReads 2 of these genesCBLSPRED1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesRNU4-2TFE3About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesIGF1About this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesDNAJC21About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesMAN2B1About this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesTUBB3About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesCEP19About this report →
- Thyroid CancerReads 2 of these genesMEN1SECISBP2About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesGLRX5About this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesSNRPNAbout this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- Coffin-Siris SyndromeReads 1 of these genesARID2About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesFGF8SNRPNAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesDMPKSPRED1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesSTILAbout this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesAHCYAbout this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesTUBG1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesSHHAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesSPG11About this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTRIM32About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPNKPAbout this report →
- Dilated CardiomyopathyReads 1 of these genesSYNE1About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesSPG11About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesSUCLG1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSBDSAbout this report →
Läs generna kopplade till Short attention span, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test159 gener kopplade till Short attention span
Förändringar i dessa gener orsakar sällsynta tillstånd där Short attention span förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| ARID2AT-rich interaction domain 2 | Alltid | I 1 tillstånd |
| ATP9AATPase phospholipid transporting 9A | Alltid | I 1 tillstånd |
| CC2D1Acoiled-coil and C2 domain containing 1A | Alltid | I 1 tillstånd |
| CHD8chromodomain helicase DNA binding protein 8 | Alltid | I 1 tillstånd |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | Alltid | I 1 tillstånd |
| IGF1insulin like growth factor 1 | Alltid | I 2 tillstånd |
| KDM6Blysine demethylase 6B | Alltid | I 1 tillstånd |
| LRRC7leucine rich repeat containing 7 | Alltid | I 1 tillstånd |
| PRMT7protein arginine methyltransferase 7 | Alltid | I 1 tillstånd |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Alltid | I 1 tillstånd |
| SLC13A1solute carrier family 13 member 1 | Alltid | I 1 tillstånd |
| NF1neurofibromin 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| RNU4-2RNA, U4 small nuclear 2 | Mycket ofta (80–99 %) | I 1 tillstånd |
| AASSaminoadipate-semialdehyde synthase | Ofta (30–79 %) | I 2 tillstånd |
| AHCYadenosylhomocysteinase | Ofta (30–79 %) | I 1 tillstånd |
| ARL6ARF like GTPase 6 | Ofta (30–79 %) | I 1 tillstånd |
| ARSAarylsulfatase A | Ofta (30–79 %) | I 2 tillstånd |
| ATP13A2ATPase cation transporting 13A2 | Ofta (30–79 %) | I 1 tillstånd |
| BBIP1BBSome interacting protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| BBS1Bardet-Biedl syndrome 1 | Ofta (30–79 %) | I 1 tillstånd |
| BBS10Bardet-Biedl syndrome 10 | Ofta (30–79 %) | I 1 tillstånd |
| BBS12Bardet-Biedl syndrome 12 | Ofta (30–79 %) | I 1 tillstånd |
| BBS2Bardet-Biedl syndrome 2 | Ofta (30–79 %) | I 1 tillstånd |
| BBS4Bardet-Biedl syndrome 4 | Ofta (30–79 %) | I 1 tillstånd |
| BBS5Bardet-Biedl syndrome 5 | Ofta (30–79 %) | I 1 tillstånd |
| BBS7Bardet-Biedl syndrome 7 | Ofta (30–79 %) | I 1 tillstånd |
| BBS9Bardet-Biedl syndrome 9 | Ofta (30–79 %) | I 1 tillstånd |
| CBLCbl proto-oncogene | Ofta (30–79 %) | I 1 tillstånd |
| CDONcell adhesion associated, oncogene regulated | Ofta (30–79 %) | I 1 tillstånd |
| CEP19centrosomal protein 19 | Ofta (30–79 %) | I 1 tillstånd |
| CEP290centrosomal protein 290 | Ofta (30–79 %) | I 1 tillstånd |
| CFAP418cilia and flagella associated protein 418 | Ofta (30–79 %) | I 1 tillstånd |
| COQ5coenzyme Q5, methyltransferase | Ofta (30–79 %) | I 1 tillstånd |
| CRIPTOcripto, EGF-CFC family member | Ofta (30–79 %) | I 1 tillstånd |
| DISP1dispatched RND transporter family member 1 | Ofta (30–79 %) | I 1 tillstånd |
| DLL1delta like canonical Notch ligand 1 | Ofta (30–79 %) | I 1 tillstånd |
| DMPKDM1 protein kinase | Ofta (30–79 %) | I 1 tillstånd |
| ELNelastin | Ofta (30–79 %) | I 1 tillstånd |
| FGF8fibroblast growth factor 8 | Ofta (30–79 %) | I 1 tillstånd |
| FOXH1forkhead box H1 | Ofta (30–79 %) | I 1 tillstånd |
Visa 119 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| FOXP1forkhead box P1 | Ofta (30–79 %) | I 1 tillstånd |
| GAS1growth arrest specific 1 | Ofta (30–79 %) | I 1 tillstånd |
| GLI2GLI family zinc finger 2 | Ofta (30–79 %) | I 1 tillstånd |
| GLRX5glutaredoxin 5 | Ofta (30–79 %) | I 1 tillstånd |
| GRIA4glutamate ionotropic receptor AMPA type subunit 4 | Ofta (30–79 %) | I 1 tillstånd |
| HIVEP2HIVEP zinc finger 2 | Ofta (30–79 %) | I 1 tillstånd |
| IFT172intraflagellar transport 172 | Ofta (30–79 %) | I 1 tillstånd |
| IFT27intraflagellar transport 27 | Ofta (30–79 %) | I 1 tillstånd |
| IFT74intraflagellar transport 74 | Ofta (30–79 %) | I 1 tillstånd |
| KMT2Alysine methyltransferase 2A | Ofta (30–79 %) | I 1 tillstånd |
| LZTFL1leucine zipper transcription factor like 1 | Ofta (30–79 %) | I 1 tillstånd |
| MAN2B1mannosidase alpha class 2B member 1 | Ofta (30–79 %) | I 1 tillstånd |
| MBD5methyl-CpG binding domain protein 5 | Ofta (30–79 %) | I 1 tillstånd |
| MID1midline 1 | Ofta (30–79 %) | I 1 tillstånd |
| MKKSMKKS centrosomal shuttling protein | Ofta (30–79 %) | I 1 tillstånd |
| MKS1MKS transition zone complex subunit 1 | Ofta (30–79 %) | I 1 tillstånd |
| MLXIPLMLX interacting protein like | Ofta (30–79 %) | I 1 tillstånd |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Ofta (30–79 %) | I 1 tillstånd |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Ofta (30–79 %) | I 1 tillstånd |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Ofta (30–79 %) | I 1 tillstånd |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Ofta (30–79 %) | I 1 tillstånd |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Ofta (30–79 %) | I 1 tillstånd |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Ofta (30–79 %) | I 1 tillstånd |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Ofta (30–79 %) | I 1 tillstånd |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Ofta (30–79 %) | I 1 tillstånd |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Ofta (30–79 %) | I 1 tillstånd |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Ofta (30–79 %) | I 1 tillstånd |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Ofta (30–79 %) | I 1 tillstånd |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Ofta (30–79 %) | I 1 tillstånd |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Ofta (30–79 %) | I 1 tillstånd |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Ofta (30–79 %) | I 1 tillstånd |
| NODALnodal growth differentiation factor | Ofta (30–79 %) | I 1 tillstånd |
| NPHP1nephrocystin 1 | Ofta (30–79 %) | I 1 tillstånd |
| OCA2OCA2 melanosomal transmembrane protein | Ofta (30–79 %) | I 1 tillstånd |
| PAK3p21 (RAC1) activated kinase 3 | Ofta (30–79 %) | I 1 tillstånd |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Ofta (30–79 %) | I 1 tillstånd |
| PRNPprion protein (Kanno blood group) | Ofta (30–79 %) | I 1 tillstånd |
| PSAPprosaposin | Ofta (30–79 %) | I 2 tillstånd |
| PTCH1patched 1 | Ofta (30–79 %) | I 1 tillstånd |
| PTENphosphatase and tensin homolog | Ofta (30–79 %) | I 1 tillstånd |
| PUS7pseudouridine synthase 7 | Ofta (30–79 %) | I 1 tillstånd |
| SCAPERS-phase cyclin A associated protein in the ER | Ofta (30–79 %) | I 1 tillstånd |
| SCLT1sodium channel and clathrin linker 1 | Ofta (30–79 %) | I 1 tillstånd |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Ofta (30–79 %) | I 1 tillstånd |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | Ofta (30–79 %) | I 1 tillstånd |
| SHHsonic hedgehog signaling molecule | Ofta (30–79 %) | I 1 tillstånd |
| SIX3SIX homeobox 3 | Ofta (30–79 %) | I 1 tillstånd |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Ofta (30–79 %) | I 1 tillstånd |
| SOBPsine oculis binding protein homolog | Ofta (30–79 %) | I 1 tillstånd |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Ofta (30–79 %) | I 1 tillstånd |
| SRPK3SRSF protein kinase 3 | Ofta (30–79 %) | I 1 tillstånd |
| STILSTIL centriolar assembly protein | Ofta (30–79 %) | I 1 tillstånd |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| TFE3transcription factor binding to IGHM enhancer 3 | Ofta (30–79 %) | I 1 tillstånd |
| TGIF1TGFB induced factor homeobox 1 | Ofta (30–79 %) | I 1 tillstånd |
| TRIM32tripartite motif containing 32 | Ofta (30–79 %) | I 1 tillstånd |
| TTC8tetratricopeptide repeat domain 8 | Ofta (30–79 %) | I 1 tillstånd |
| UBE3Aubiquitin protein ligase E3A | Ofta (30–79 %) | I 2 tillstånd |
| WDPCPWD repeat containing planar cell polarity effector | Ofta (30–79 %) | I 1 tillstånd |
| ZIC2Zic family zinc finger 2 | Ofta (30–79 %) | I 1 tillstånd |
| ABCD1ATP binding cassette subfamily D member 1 | Ibland (5–29 %) | I 1 tillstånd |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Ibland (5–29 %) | I 1 tillstånd |
| ATP10AATPase phospholipid transporting 10A (putative) | Ibland (5–29 %) | I 1 tillstånd |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Ibland (5–29 %) | I 1 tillstånd |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Ibland (5–29 %) | I 1 tillstånd |
| CLTCclathrin heavy chain | Ibland (5–29 %) | I 1 tillstånd |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Ibland (5–29 %) | I 1 tillstånd |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Ibland (5–29 %) | I 1 tillstånd |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Ibland (5–29 %) | I 1 tillstånd |
| EFL1elongation factor like GTPase 1 | Ibland (5–29 %) | I 1 tillstånd |
| FOCADfocadhesin | Ibland (5–29 %) | I 1 tillstånd |
| FOXP2forkhead box P2 | Ibland (5–29 %) | I 1 tillstånd |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Ibland (5–29 %) | I 1 tillstånd |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Ibland (5–29 %) | I 2 tillstånd |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Ibland (5–29 %) | I 1 tillstånd |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Ibland (5–29 %) | I 3 tillstånd |
| HTRA2HtrA serine peptidase 2 | Ibland (5–29 %) | I 1 tillstånd |
| LRRK2leucine rich repeat kinase 2 | Ibland (5–29 %) | I 1 tillstånd |
| MEN1menin 1 | Ibland (5–29 %) | I 1 tillstånd |
| NIPA1NIPA magnesium transporter 1 | Ibland (5–29 %) | I 1 tillstånd |
| NIPA2NIPA magnesium transporter 2 | Ibland (5–29 %) | I 1 tillstånd |
| NTRK1neurotrophic receptor tyrosine kinase 1 | Ibland (5–29 %) | I 1 tillstånd |
| PARK7Parkinsonism associated deglycase | Ibland (5–29 %) | I 1 tillstånd |
| PCDH19protocadherin 19 | Ibland (5–29 %) | I 1 tillstånd |
| PINK1PTEN induced kinase 1 | Ibland (5–29 %) | I 1 tillstånd |
| PLA2G6phospholipase A2 group VI | Ibland (5–29 %) | I 2 tillstånd |
| PNKPpolynucleotide kinase 3'-phosphatase | Ibland (5–29 %) | I 1 tillstånd |
| PODXLpodocalyxin like | Ibland (5–29 %) | I 1 tillstånd |
| PRKNparkin RBR E3 ubiquitin protein ligase | Ibland (5–29 %) | I 1 tillstånd |
| PURApurine rich element binding protein A | Ibland (5–29 %) | I 1 tillstånd |
| SATB1SATB homeobox 1 | Ibland (5–29 %) | I 1 tillstånd |
| SBDSSBDS ribosome maturation factor | Ibland (5–29 %) | I 1 tillstånd |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Ibland (5–29 %) | I 1 tillstånd |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Ibland (5–29 %) | I 1 tillstånd |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Ibland (5–29 %) | I 1 tillstånd |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Ibland (5–29 %) | I 1 tillstånd |
| SECISBP2SECIS binding protein 2 | Ibland (5–29 %) | I 1 tillstånd |
| SIN3ASIN3 transcription regulator family member A | Ibland (5–29 %) | I 1 tillstånd |
| SIN3BSIN3 transcription regulator family member B | Ibland (5–29 %) | I 1 tillstånd |
| SNCAsynuclein alpha | Ibland (5–29 %) | I 1 tillstånd |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Ibland (5–29 %) | I 1 tillstånd |
| SPRED1sprouty related EVH1 domain containing 1 | Ibland (5–29 %) | I 1 tillstånd |
| SRCAPSnf2 related CREBBP activator protein | Ibland (5–29 %) | I 1 tillstånd |
| SRPX2sushi repeat containing protein X-linked 2 | Ibland (5–29 %) | I 2 tillstånd |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Ibland (5–29 %) | I 1 tillstånd |
| SYNJ1synaptojanin 1 | Ibland (5–29 %) | I 1 tillstånd |
| TAOK1TAO kinase 1 | Ibland (5–29 %) | I 1 tillstånd |
| TUBB3tubulin beta 3 class III | Ibland (5–29 %) | I 1 tillstånd |
| TUBG1tubulin gamma 1 | Ibland (5–29 %) | I 1 tillstånd |
| UCHL1ubiquitin C-terminal hydrolase L1 | Ibland (5–29 %) | I 1 tillstånd |
| VPS13Avacuolar protein sorting 13 homolog A | Ibland (5–29 %) | I 1 tillstånd |
| VPS13Cvacuolar protein sorting 13 homolog C | Ibland (5–29 %) | I 1 tillstånd |
| NKX2-1NK2 homeobox 1 | Sällan (1–4%) | I 1 tillstånd |
| SPTBN1spectrin beta, non-erythrocytic 1 | Sällan (1–4%) | I 1 tillstånd |
| ASPNATaspartate N-acetyltransferase | Inte registrerat | I 1 tillstånd |
| AUHAU RNA binding methylglutaconyl-CoA hydratase | Inte registrerat | I 1 tillstånd |
| CREBBPCREB binding lysine acetyltransferase | Inte registrerat | I 1 tillstånd |
| EP300EP300 lysine acetyltransferase | Inte registrerat | I 1 tillstånd |
| FBXO11F-box protein 11 | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
Mer specifika egenskaper
Bredare egenskaper
Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.21-777c9289.
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