Tunnus
Abnormality on pulmonary function testing
Any anomaly measure by pulmonary function testing, which includes spirometry, measures of diffusing capacity, and plethysmography.
Kokkuvõte
- Teised nimetused
- Abnormal pulmonary function test
- Kehasüsteem
- Abnormality of the respiratory system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Abnormality on pulmonary function testing, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test46 geeni on seotud tunnusega Abnormality on pulmonary function testing
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Abnormality on pulmonary function testing. 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 |
|---|---|---|
| ACTA1actin alpha 1, skeletal muscle | Sageli (30–79%) | 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 |
| HLA-DPB1major histocompatibility complex, class II, DP beta 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 |
| PFN1profilin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PRPHperipherin | Sageli (30–79%) | Esineb 1 haiguses |
| SELENONselenoprotein N | Sageli (30–79%) | Esineb 1 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 1 haiguses |
| UNC13Aunc-13 homolog A | Sageli (30–79%) | Esineb 1 haiguses |
| VAPBVAMP associated protein B and C | Sageli (30–79%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Sageli (30–79%) | Esineb 1 haiguses |
| AKT1AKT serine/threonine kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| BAP1BRCA1 associated deubiquitinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Harva (1–4%) | Esineb 1 haiguses |
| PDGFBplatelet derived growth factor subunit B | Harva (1–4%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Harva (1–4%) | Esineb 1 haiguses |
Näita veel 6 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Harva (1–4%) | Esineb 1 haiguses |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Harva (1–4%) | Esineb 1 haiguses |
| SMOsmoothened, frizzled class receptor | Harva (1–4%) | Esineb 1 haiguses |
| SUFUSUFU negative regulator of hedgehog signaling | Harva (1–4%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Harva (1–4%) | Esineb 1 haiguses |
| TRAF7TNF receptor associated factor 7 | Harva (1–4%) | 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