All individuals with variants in gene PXDNL

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00011678 - - detected possibly causative variant but have not yet sufficient evidence to publish - please contact me M - Germany - - 1 - - polyposis colorectal adenomatous polyposis 1 1 Sukanya Horpaopan
00016291 - - detected possibly causative variant but have not yet sufficient evidence to publish - please contact me F ? Germany - - 1 - - polyposis colorectal adenomatous polyposis 1 1 Sukanya Horpaopan
00016292 - - detected possibly causative variant but have not yet sufficient evidence to publish - please contact me M ? Germany - - 1 - - polyposis colorectal adenomatous polyposis 1 1 Sukanya Horpaopan
00016293 - - detected possibly causative variant but have not yet sufficient evidence to publish - please contact me F ? Germany - - 1 - - polyposis colorectal adenomatous polyposis 1 1 Sukanya Horpaopan
00016294 - - detected possibly causative variant but have not yet sufficient evidence to publish - please contact me M ? Germany - - 1 - - CRC familial colorectal cancer 1 1 Sukanya Horpaopan
00209009 28771251-Pat71 PubMed: Lionel 2018 - - - Canada - - - - - ? - 1 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.