Tunnus
Paralysis
Paralysis of voluntary muscles means loss of contraction due to interruption of one or more motor pathways from the brain to the muscle fibers. Although the word paralysis is often used interchangeably to mean either complete or partial loss of muscle strength, it is preferable to use paralysis or plegia for complete or severe loss of muscle strength, and paresis for partial or slight loss. Motor paralysis results from deficits of the upper motor neurons (corticospinal, corticobulbar, or subcorticospinal). Motor paralysis is often accompanied by an impairment in the facility of movement.
Kokkuvõte
- Teised nimetused
- Inability to move
- Kehasüsteem
- Abnormality of the nervous system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Paralysis, and the rest of your genome, with one test.
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Telli oma Genome Test61 geeni on seotud tunnusega Paralysis
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Paralysis. 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 |
|---|---|---|
| BORCS8BLOC-1 related complex subunit 8 | Alati | Esineb 1 haiguses |
| FDXRferredoxin reductase | Alati | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alati | Esineb 2 haiguses |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Väga sageli (80–99%) | Esineb 2 haiguses |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANGangiogenin | Sageli (30–79%) | Esineb 1 haiguses |
| ANXA11annexin A11 | Sageli (30–79%) | Esineb 1 haiguses |
| ATXN2ataxin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CCNFcyclin F | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP410cilia and flagella associated protein 410 | Sageli (30–79%) | Esineb 1 haiguses |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Sageli (30–79%) | Esineb 1 haiguses |
| CHMP2Bcharged multivesicular body protein 2B | Sageli (30–79%) | Esineb 1 haiguses |
| DAOD-amino acid oxidase | Sageli (30–79%) | Esineb 1 haiguses |
| DCTN1dynactin subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| FIG4FIG4 phosphoinositide 5-phosphatase | Sageli (30–79%) | Esineb 1 haiguses |
| FUSFUS RNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| GLE1GLE1 RNA export mediator | Sageli (30–79%) | Esineb 1 haiguses |
| GLT8D1glycosyltransferase 8 domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Sageli (30–79%) | Esineb 1 haiguses |
| LRP12LDL receptor related protein 12 | Sageli (30–79%) | Esineb 1 haiguses |
| MATR3matrin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| NEFHneurofilament heavy chain | Sageli (30–79%) | Esineb 1 haiguses |
| NEK1NIMA related kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| OPTNoptineurin | Sageli (30–79%) | Esineb 1 haiguses |
| PDCD10programmed cell death 10 | Sageli (30–79%) | Esineb 1 haiguses |
| PFN1profilin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PRPHperipherin | Sageli (30–79%) | Esineb 1 haiguses |
| SLC2A1solute carrier family 2 member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SOD1superoxide dismutase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SQSTM1sequestosome 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TAF15TATA-box binding protein associated factor 15 | Sageli (30–79%) | Esineb 1 haiguses |
| TARDBPTAR DNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Sageli (30–79%) | Esineb 1 haiguses |
| UBQLN2ubiquilin 2 | Sageli (30–79%) | Esineb 2 haiguses |
| UNC13Aunc-13 homolog A | Sageli (30–79%) | Esineb 1 haiguses |
| VAPBVAMP associated protein B and C | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 21 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| VCPvalosin containing protein | Sageli (30–79%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCHEbutyrylcholinesterase | Harva (1–4%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Harva (1–4%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Harva (1–4%) | Esineb 2 haiguses |
| ALADaminolevulinate dehydratase | Pole registreeritud | Esineb 1 haiguses |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Pole registreeritud | Esineb 1 haiguses |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Pole registreeritud | Esineb 1 haiguses |
| CD59CD59 molecule (CD59 blood group) | Pole registreeritud | Esineb 1 haiguses |
| CNTNAP1contactin associated protein 1 | Pole registreeritud | Esineb 1 haiguses |
| EEF2eukaryotic translation elongation factor 2 | Pole registreeritud | Esineb 1 haiguses |
| GM2Aganglioside GM2 activator | Pole registreeritud | Esineb 1 haiguses |
| HK1hexokinase 1 | Pole registreeritud | Esineb 1 haiguses |
| HMBShydroxymethylbilane synthase | Pole registreeritud | Esineb 1 haiguses |
| HSPB1heat shock protein family B (small) member 1 | Pole registreeritud | Esineb 1 haiguses |
| HSPB8heat shock protein family B (small) member 8 | Pole registreeritud | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Pole registreeritud | Esineb 1 haiguses |
| PPOXprotoporphyrinogen oxidase | Pole registreeritud | Esineb 1 haiguses |
| SLC25A19solute carrier family 25 member 19 | Pole registreeritud | Esineb 1 haiguses |
| TRPM7transient receptor potential cation channel subfamily M member 7 | 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.
Kitsamad tunnused
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