Tunnus
Increased circulating potassium concentration
Kliiniline nimetus: Hyperkalemia
The concentration of potassium(1+) in the blood circulation is above the upper limit of normal.
Kokkuvõte
- Teised nimetused
- Elevated potassium(1+) concentration, Elevated potassium(1+) level, Elevated potassium(1+) level in blood, Increased potassium(1+) concentration, Increased potassium(1+) level, Increased potassium(1+) level in blood
- Kehasüsteem
- Laboratory abnormality
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Increased circulating potassium concentration, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test42 geeni on seotud tunnusega Increased circulating potassium concentration
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Increased circulating potassium concentration. 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 |
|---|---|---|
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Alati | Esineb 3 haiguses |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Alati | Esineb 1 haiguses |
| OAS22'-5'-oligoadenylate synthetase 2 | Alati | Esineb 1 haiguses |
| POLG2DNA polymerase gamma 2, accessory subunit | Alati | Esineb 1 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Alati | Esineb 2 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Alati | Esineb 2 haiguses |
| SLC2A1solute carrier family 2 member 1 | Alati | Esineb 1 haiguses |
| SLC4A2solute carrier family 4 member 2 | Alati | Esineb 1 haiguses |
| WNK1WNK lysine deficient protein kinase 1 | Alati | Esineb 1 haiguses |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Väga sageli (80–99%) | Esineb 2 haiguses |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Väga sageli (80–99%) | Esineb 2 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 |
| NNTnicotinamide nucleotide transhydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Sageli (30–79%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sageli (30–79%) | Esineb 2 haiguses |
| SEC61A1SEC61 translocon subunit alpha 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC30A9solute carrier family 30 member 9 | Sageli (30–79%) | Esineb 1 haiguses |
| STARsteroidogenic acute regulatory protein | Sageli (30–79%) | Esineb 1 haiguses |
| TXNRD2thioredoxin reductase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ALDOAaldolase, fructose-bisphosphate A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Mõnikord (5–29%) | Esineb 2 haiguses |
| LPIN1lipin 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Mõnikord (5–29%) | Esineb 1 haiguses |
| OBSCNobscurin, cytoskeletal calmodulin and titin-interacting RhoGEF | Mõnikord (5–29%) | Esineb 1 haiguses |
| PAX2paired box 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PBX1PBX homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Harva (1–4%) | Esineb 1 haiguses |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Harva (1–4%) | Esineb 1 haiguses |
| CA12carbonic anhydrase 12 | Pole registreeritud | Esineb 1 haiguses |
| CUL3cullin 3 | Pole registreeritud | Esineb 1 haiguses |
| INVSinversin | Pole registreeritud | Esineb 1 haiguses |
| KLHL3kelch like family member 3 | Pole registreeritud | Esineb 1 haiguses |
| NFKB2nuclear factor kappa B subunit 2 | Pole registreeritud | Esineb 1 haiguses |
| SAMD9sterile alpha motif domain containing 9 | Pole registreeritud | Esineb 1 haiguses |
Näita veel 2 geeni
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.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast