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Tunnus
Low blood sodium levels
Kliiniline nimetus: Hyponatremia
The concentration of sodium in the blood circulation is below the lower limit of normal.
Kokkuvõte
- Teised nimetused
- Decreased sodium(1+) concentration, Decreased sodium(1+) level, Decreased sodium(1+) level in blood, Reduced sodium(1+) concentration, Reduced sodium(1+) level, Reduced sodium(1+) level in blood
- Kehasüsteem
- Laboratory abnormality
Low blood sodium levelsHP:0002902
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Read the genes linked to Low blood sodium levels, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test62 geeni on seotud tunnusega Low blood sodium levels
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Low blood sodium levels. 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 |
|---|---|---|
| ATIC5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Alati | Esineb 1 haiguses |
| AVPR2arginine vasopressin receptor 2 | Alati | Esineb 1 haiguses |
| CTNScystinosin, lysosomal cystine transporter | Alati | Esineb 2 haiguses |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Alati | Esineb 3 haiguses |
| NUP214nucleoporin 214 | Alati | Esineb 1 haiguses |
| PLVAPplasmalemma vesicle associated protein | Alati | Esineb 1 haiguses |
| SARS2seryl-tRNA synthetase 2, mitochondrial | Alati | Esineb 1 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Alati | Esineb 2 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Alati | Esineb 2 haiguses |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NFKB2nuclear factor kappa B subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Väga sageli (80–99%) | Esineb 1 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| TBX19T-box transcription factor 19 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| BSNDbarttin CLCNK type accessory subunit beta | Sageli (30–79%) | Esineb 2 haiguses |
| CLCNKAchloride voltage-gated channel Ka | Sageli (30–79%) | Esineb 2 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Sageli (30–79%) | Esineb 2 haiguses |
| DZIP1LDAZ interacting zinc finger protein 1 like | Sageli (30–79%) | Esineb 1 haiguses |
| GEMIN4gem nuclear organelle associated protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| MC2Rmelanocortin 2 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| MRAPmelanocortin 2 receptor accessory protein | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFB8NADH:ubiquinone oxidoreductase subunit B8 | Sageli (30–79%) | Esineb 1 haiguses |
| NNTnicotinamide nucleotide transhydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Sageli (30–79%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Sageli (30–79%) | Esineb 1 haiguses |
| RRAGDRas related GTP binding D | Sageli (30–79%) | Esineb 1 haiguses |
| SETD2SET domain containing 2, histone lysine methyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| STARsteroidogenic acute regulatory protein | Sageli (30–79%) | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TICAM1TIR domain containing adaptor molecule 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TLR3toll like receptor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TRAF3TNF receptor associated factor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TSFMTs translation elongation factor, mitochondrial | Sageli (30–79%) | Esineb 1 haiguses |
| TXNRD2thioredoxin reductase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| UNC93B1unc-93B1 regulator of TLR signaling | Sageli (30–79%) | Esineb 1 haiguses |
| ALADaminolevulinate dehydratase | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 22 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD4CD4 molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ELP1elongator acetyltransferase complex subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOCADfocadhesin | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMBShydroxymethylbilane synthase | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL36RNinterleukin 36 receptor antagonist | Mõnikord (5–29%) | Esineb 1 haiguses |
| IRF4interferon regulatory factor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LYSTlysosomal trafficking regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| PAX2paired box 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PBX1PBX homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPOXprotoporphyrinogen oxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Harva (1–4%) | Esineb 1 haiguses |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Harva (1–4%) | Esineb 1 haiguses |
| CA12carbonic anhydrase 12 | Pole registreeritud | Esineb 1 haiguses |
| MAGED2MAGE family member D2 | Pole registreeritud | Esineb 1 haiguses |
| PRF1perforin 1 | Pole registreeritud | Esineb 1 haiguses |
| SAMD9sterile alpha motif domain containing 9 | Pole registreeritud | Esineb 1 haiguses |
| SLC26A3solute carrier family 26 member 3 | Pole registreeritud | Esineb 1 haiguses |
| TDP2tyrosyl-DNA phosphodiesterase 2 | 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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Logi sisseKüsiAlustaalates 449 $
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast