Tunnus
Obstructive azoospermia
Absence of any measurable level of sperm in his semen, resulting from post-testicular obstruction or retrograde ejaculation. This can be differentiated from obstructive azoospermia on the basis of testicular biopsy.
Kokkuvõte
- Kehasüsteem
- Abnormality of the genitourinary system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Obstructive azoospermia, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test39 geeni on seotud tunnusega Obstructive azoospermia
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Obstructive azoospermia. 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 |
|---|---|---|
| CLDN2claudin 2 | Alati | Esineb 1 haiguses |
| ADGRG2adhesion G protein-coupled receptor G2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CFTRCF transmembrane conductance regulator | Väga sageli (80–99%) | Esineb 2 haiguses |
| CATIPciliogenesis associated TTC17 interacting protein | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC34coiled-coil domain containing 34 | Sageli (30–79%) | Esineb 1 haiguses |
| CT55cancer/testis antigen 55 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAH10dynein axonemal heavy chain 10 | Sageli (30–79%) | Esineb 1 haiguses |
| DNHD1dynein heavy chain domain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| FANCMFA complementation group M | Sageli (30–79%) | Esineb 1 haiguses |
| FBXO43F-box protein 43 | Sageli (30–79%) | Esineb 1 haiguses |
| GCNAgerm cell nuclear acidic peptidase | Sageli (30–79%) | Esineb 1 haiguses |
| KLHL10kelch like family member 10 | Sageli (30–79%) | Esineb 1 haiguses |
| MEIOBmeiosis specific with OB-fold | Sageli (30–79%) | Esineb 1 haiguses |
| MOV10L1Mov10 like RNA helicase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MSH5mutS homolog 5 | Sageli (30–79%) | Esineb 1 haiguses |
| NANOS1nanos C2HC-type zinc finger 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PDHA2pyruvate dehydrogenase E1 subunit alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PNLDC1PARN like ribonuclease domain containing exonuclease 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RBBP7RB binding protein 7, chromatin remodeling factor | Sageli (30–79%) | Esineb 1 haiguses |
| RNF212ring finger protein 212 | Sageli (30–79%) | Esineb 1 haiguses |
| RPL10Lribosomal protein L10 like | Sageli (30–79%) | Esineb 1 haiguses |
| SHOC1shortage in chiasmata 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SOHLH1spermatogenesis and oogenesis specific basic helix-loop-helix 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SPAG17sperm associated antigen 17 | Sageli (30–79%) | Esineb 1 haiguses |
| SPINK2serine peptidase inhibitor Kazal type 2 | Sageli (30–79%) | Esineb 1 haiguses |
| STAG3STAG3 cohesin complex component | Sageli (30–79%) | Esineb 1 haiguses |
| SYCE1synaptonemal complex central element protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SYCP3synaptonemal complex protein 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TAF4BTATA-box binding protein associated factor 4b | Sageli (30–79%) | Esineb 1 haiguses |
| TDRD9tudor domain containing 9 | Sageli (30–79%) | Esineb 1 haiguses |
| TERB1telomere repeat binding bouquet formation protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TERB2telomere repeat binding bouquet formation protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TEX11testis expressed 11 | Sageli (30–79%) | Esineb 1 haiguses |
| TEX14testis expressed 14, intercellular bridge forming factor | Sageli (30–79%) | Esineb 1 haiguses |
| TEX15testis expressed 15, meiosis and synapsis associated | Sageli (30–79%) | Esineb 1 haiguses |
| XRCC2X-ray repair cross complementing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ZMYND15zinc finger MYND-type containing 15 | Sageli (30–79%) | Esineb 1 haiguses |
| ZSWIM7zinc finger SWIM-type containing 7 | Sageli (30–79%) | 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.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast