Atlas이런 분들을 위해과학적 근거제품연구 성과
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형질
Short attention span
Reduced attention span characterized by distractibility and impulsivity.
요약
- 다른 명칭
- Poor attention span, Problem paying attention, Easily distracted, Easy distractibility, High distractibility
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
이 페이지의 데이터
페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/short-attention-span.json"
page <- fromJSON(url)
page$trait$nameShort attention spanHP:0000736
Atlas이런 분들을 위해과학적 근거제품연구 성과
로그인질문하기유전체를 시퀀싱하세요↗
Short attention span과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기82 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 →
Short attention span과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
$449부터배송비 무료 · 결과는 6~8주 내 제공
내 Genome Test 받기연관 유전자 159개: Short attention span
이 유전자들의 변화는 Short attention span 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| ARID2AT-rich interaction domain 2 | 항상 | 질환 1개에서 나타남 |
| ATP9AATPase phospholipid transporting 9A | 항상 | 질환 1개에서 나타남 |
| CC2D1Acoiled-coil and C2 domain containing 1A | 항상 | 질환 1개에서 나타남 |
| CHD8chromodomain helicase DNA binding protein 8 | 항상 | 질환 1개에서 나타남 |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | 항상 | 질환 1개에서 나타남 |
| IGF1insulin like growth factor 1 | 항상 | 질환 2개에서 나타남 |
| KDM6Blysine demethylase 6B | 항상 | 질환 1개에서 나타남 |
| LRRC7leucine rich repeat containing 7 | 항상 | 질환 1개에서 나타남 |
| PRMT7protein arginine methyltransferase 7 | 항상 | 질환 1개에서 나타남 |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | 항상 | 질환 1개에서 나타남 |
| SLC13A1solute carrier family 13 member 1 | 항상 | 질환 1개에서 나타남 |
| NF1neurofibromin 1 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| RNU4-2RNA, U4 small nuclear 2 | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| AASSaminoadipate-semialdehyde synthase | 자주 (30–79%) | 질환 2개에서 나타남 |
| AHCYadenosylhomocysteinase | 자주 (30–79%) | 질환 1개에서 나타남 |
| ARL6ARF like GTPase 6 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ARSAarylsulfatase A | 자주 (30–79%) | 질환 2개에서 나타남 |
| ATP13A2ATPase cation transporting 13A2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBIP1BBSome interacting protein 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS1Bardet-Biedl syndrome 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS10Bardet-Biedl syndrome 10 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS12Bardet-Biedl syndrome 12 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS2Bardet-Biedl syndrome 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS4Bardet-Biedl syndrome 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS5Bardet-Biedl syndrome 5 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS7Bardet-Biedl syndrome 7 | 자주 (30–79%) | 질환 1개에서 나타남 |
| BBS9Bardet-Biedl syndrome 9 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CBLCbl proto-oncogene | 자주 (30–79%) | 질환 1개에서 나타남 |
| CDONcell adhesion associated, oncogene regulated | 자주 (30–79%) | 질환 1개에서 나타남 |
| CEP19centrosomal protein 19 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CEP290centrosomal protein 290 | 자주 (30–79%) | 질환 1개에서 나타남 |
| CFAP418cilia and flagella associated protein 418 | 자주 (30–79%) | 질환 1개에서 나타남 |
| COQ5coenzyme Q5, methyltransferase | 자주 (30–79%) | 질환 1개에서 나타남 |
| CRIPTOcripto, EGF-CFC family member | 자주 (30–79%) | 질환 1개에서 나타남 |
| DISP1dispatched RND transporter family member 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| DLL1delta like canonical Notch ligand 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| DMPKDM1 protein kinase | 자주 (30–79%) | 질환 1개에서 나타남 |
| ELNelastin | 자주 (30–79%) | 질환 1개에서 나타남 |
| FGF8fibroblast growth factor 8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| FOXH1forkhead box H1 | 자주 (30–79%) | 질환 1개에서 나타남 |
유전자 119개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| FOXP1forkhead box P1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GAS1growth arrest specific 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GLI2GLI family zinc finger 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GLRX5glutaredoxin 5 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GRIA4glutamate ionotropic receptor AMPA type subunit 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| HIVEP2HIVEP zinc finger 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IFT172intraflagellar transport 172 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IFT27intraflagellar transport 27 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IFT74intraflagellar transport 74 | 자주 (30–79%) | 질환 1개에서 나타남 |
| KMT2Alysine methyltransferase 2A | 자주 (30–79%) | 질환 1개에서 나타남 |
| LZTFL1leucine zipper transcription factor like 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MAN2B1mannosidase alpha class 2B member 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MBD5methyl-CpG binding domain protein 5 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MID1midline 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MKKSMKKS centrosomal shuttling protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| MKS1MKS transition zone complex subunit 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MLXIPLMLX interacting protein like | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | 자주 (30–79%) | 질환 1개에서 나타남 |
| NODALnodal growth differentiation factor | 자주 (30–79%) | 질환 1개에서 나타남 |
| NPHP1nephrocystin 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| OCA2OCA2 melanosomal transmembrane protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| PAK3p21 (RAC1) activated kinase 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | 자주 (30–79%) | 질환 1개에서 나타남 |
| PRNPprion protein (Kanno blood group) | 자주 (30–79%) | 질환 1개에서 나타남 |
| PSAPprosaposin | 자주 (30–79%) | 질환 2개에서 나타남 |
| PTCH1patched 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| PTENphosphatase and tensin homolog | 자주 (30–79%) | 질환 1개에서 나타남 |
| PUS7pseudouridine synthase 7 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SCAPERS-phase cyclin A associated protein in the ER | 자주 (30–79%) | 질환 1개에서 나타남 |
| SCLT1sodium channel and clathrin linker 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | 자주 (30–79%) | 질환 1개에서 나타남 |
| SHHsonic hedgehog signaling molecule | 자주 (30–79%) | 질환 1개에서 나타남 |
| SIX3SIX homeobox 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SOBPsine oculis binding protein homolog | 자주 (30–79%) | 질환 1개에서 나타남 |
| SPG11SPG11 vesicle trafficking associated, spatacsin | 자주 (30–79%) | 질환 1개에서 나타남 |
| SRPK3SRSF protein kinase 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| STILSTIL centriolar assembly protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TFE3transcription factor binding to IGHM enhancer 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TGIF1TGFB induced factor homeobox 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TRIM32tripartite motif containing 32 | 자주 (30–79%) | 질환 1개에서 나타남 |
| TTC8tetratricopeptide repeat domain 8 | 자주 (30–79%) | 질환 1개에서 나타남 |
| UBE3Aubiquitin protein ligase E3A | 자주 (30–79%) | 질환 2개에서 나타남 |
| WDPCPWD repeat containing planar cell polarity effector | 자주 (30–79%) | 질환 1개에서 나타남 |
| ZIC2Zic family zinc finger 2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| ABCD1ATP binding cassette subfamily D member 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ATP10AATPase phospholipid transporting 10A (putative) | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CDKN1Bcyclin dependent kinase inhibitor 1B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CDKN2Bcyclin dependent kinase inhibitor 2B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CLTCclathrin heavy chain | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| EFL1elongation factor like GTPase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FOCADfocadhesin | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FOXP2forkhead box P2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | 가끔 (5–29%) | 질환 3개에서 나타남 |
| HTRA2HtrA serine peptidase 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LRRK2leucine rich repeat kinase 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MEN1menin 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NIPA1NIPA magnesium transporter 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NIPA2NIPA magnesium transporter 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NTRK1neurotrophic receptor tyrosine kinase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PARK7Parkinsonism associated deglycase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PCDH19protocadherin 19 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PINK1PTEN induced kinase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PLA2G6phospholipase A2 group VI | 가끔 (5–29%) | 질환 2개에서 나타남 |
| PNKPpolynucleotide kinase 3'-phosphatase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PODXLpodocalyxin like | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PRKNparkin RBR E3 ubiquitin protein ligase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PURApurine rich element binding protein A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SATB1SATB homeobox 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SBDSSBDS ribosome maturation factor | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN1Asodium voltage-gated channel alpha subunit 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN1Bsodium voltage-gated channel beta subunit 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN2Asodium voltage-gated channel alpha subunit 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SCN9Asodium voltage-gated channel alpha subunit 9 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SECISBP2SECIS binding protein 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SIN3ASIN3 transcription regulator family member A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SIN3BSIN3 transcription regulator family member B | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SNCAsynuclein alpha | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SPRED1sprouty related EVH1 domain containing 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SRCAPSnf2 related CREBBP activator protein | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SRPX2sushi repeat containing protein X-linked 2 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SYNJ1synaptojanin 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TAOK1TAO kinase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TUBB3tubulin beta 3 class III | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TUBG1tubulin gamma 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| UCHL1ubiquitin C-terminal hydrolase L1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| VPS13Avacuolar protein sorting 13 homolog A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| VPS13Cvacuolar protein sorting 13 homolog C | 가끔 (5–29%) | 질환 1개에서 나타남 |
| NKX2-1NK2 homeobox 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| SPTBN1spectrin beta, non-erythrocytic 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| ASPNATaspartate N-acetyltransferase | 기록되지 않음 | 질환 1개에서 나타남 |
| AUHAU RNA binding methylglutaconyl-CoA hydratase | 기록되지 않음 | 질환 1개에서 나타남 |
| CREBBPCREB binding lysine acetyltransferase | 기록되지 않음 | 질환 1개에서 나타남 |
| EP300EP300 lysine acetyltransferase | 기록되지 않음 | 질환 1개에서 나타남 |
| FBXO11F-box protein 11 | 기록되지 않음 | 질환 1개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
하위 형질
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
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