All individuals with variants in gene CLDN16

3 entries on 1 page. Showing entries 1 - 3.
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     
00032320 - PubMed: Schueler 2015, Journal: Schueler 2015 patient, unaffected heterozygous carrier parents ? yes United Kingdom (Great Britain) - - - - - NPHPRC see paper; 11m-hepatic fibrosis; 14y-end-stage renal disease (ESRD) from NPHP; ... 1 1 Johan den Dunnen
00080833 - PubMed: Trujillano 2017 no information from parents - - - - - - - - HOMG3 Hypomagnesemia 3, renal type (OMIM:248250) 1 1 Daniel Trujillano
00293301 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
Legend   How to query  


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