Tunnus
Episodic vomiting
Paroxysmal, recurrent episodes of vomiting.
Kokkuvõte
- Teised nimetused
- Frequent vomiting
- Kehasüsteem
- Abnormality of the digestive system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Episodic vomiting, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test78 geeni on seotud tunnusega Episodic vomiting
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Episodic vomiting. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ACADVLacyl-CoA dehydrogenase very long chain | Alati | Esineb 1 haiguses |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Alati | Esineb 1 haiguses |
| APTXaprataxin | Alati | Esineb 1 haiguses |
| ARG1arginase 1 | Alati | Esineb 1 haiguses |
| COQ2coenzyme Q2, polyprenyltransferase | Alati | Esineb 1 haiguses |
| LBX1ladybird homeobox 1 | Alati | Esineb 1 haiguses |
| MAN2B2mannosidase alpha class 2B member 2 | Alati | Esineb 1 haiguses |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Alati | Esineb 1 haiguses |
| NDC1NDC1 transmembrane nucleoporin | Alati | Esineb 1 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Alati | Esineb 1 haiguses |
| SEC61A1SEC61 translocon subunit alpha 1 | Alati | Esineb 1 haiguses |
| SEL1LSEL1L adaptor subunit of SYVN1 ubiquitin ligase | Alati | Esineb 1 haiguses |
| SUOXsulfite oxidase | Alati | Esineb 1 haiguses |
| TOP2BDNA topoisomerase II beta | Alati | Esineb 1 haiguses |
| UNC13Aunc-13 homolog A | Alati | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Sageli (30–79%) | Esineb 1 haiguses |
| D2HGDHD-2-hydroxyglutarate dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| FAHfumarylacetoacetate hydrolase | Sageli (30–79%) | Esineb 1 haiguses |
| FGF13fibroblast growth factor 13 | Sageli (30–79%) | Esineb 1 haiguses |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Sageli (30–79%) | Esineb 2 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Sageli (30–79%) | Esineb 2 haiguses |
| NDUFS1NADH:ubiquinone oxidoreductase core subunit S1 | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFS7NADH:ubiquinone oxidoreductase core subunit S7 | Sageli (30–79%) | Esineb 1 haiguses |
| NEXMIFneurite extension and migration factor | Sageli (30–79%) | Esineb 1 haiguses |
| POGZpogo transposable element derived with ZNF domain | Sageli (30–79%) | Esineb 1 haiguses |
| RNH1ribonuclease/angiogenin inhibitor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A15solute carrier family 25 member 15 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC5A6solute carrier family 5 member 6 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 38 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| TTRtransthyretin | Sageli (30–79%) | Esineb 1 haiguses |
| UQCRC2ubiquinol-cytochrome c reductase core protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALADaminolevulinate dehydratase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALG11ALG11 alpha-1,2-mannosyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CA5Acarbonic anhydrase 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCM2CCM2 scaffold protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC42BPBCDC42 binding protein kinase beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDK13cyclin dependent kinase 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDK8cyclin dependent kinase 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GAMTguanidinoacetate N-methyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Mõnikord (5–29%) | Esineb 2 haiguses |
| KRIT1KRIT1 ankyrin repeat containing | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAXDNAD(P)HX dehydratase | Mõnikord (5–29%) | Esineb 1 haiguses |
| NFIXnuclear factor I X | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOTCH2NLCnotch 2 N-terminal like C | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTCornithine transcarbamylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDCD10programmed cell death 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPMT1protein tyrosine phosphatase mitochondrial 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMPD1sphingomyelin phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UNC45Aunc-45 myosin chaperone A | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZEB2zinc finger E-box binding homeobox 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MARK2microtubule affinity regulating kinase 2 | Harva (1–4%) | Esineb 1 haiguses |
| GKglycerol kinase | Pole registreeritud | Esineb 1 haiguses |
| HS3ST6heparan sulfate-glucosamine 3-sulfotransferase 6 | Pole registreeritud | Esineb 1 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Pole registreeritud | Esineb 1 haiguses |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Pole registreeritud | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Pole registreeritud | Esineb 1 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Pole registreeritud | Esineb 1 haiguses |
| MT-TCmitochondrially encoded tRNA-Cys (UGU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Pole registreeritud | Esineb 1 haiguses |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Pole registreeritud | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Pole registreeritud | Esineb 1 haiguses |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Pole registreeritud | Esineb 1 haiguses |
| NLRC4NLR family CARD domain containing 4 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast