All individuals with variants in gene CTSD

4 entries on 1 page. Showing entries 1 - 4.
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     
00148288 - - - M - (Germany) - - - - - ? Ataxia (HP:0001251); Cerebellar atrophy (HP:0001272); Retinal degeneration (HP:0000546) 1 1 IMGAG
00290327 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00395563 RP-0249 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease rod-cone dystrophy, seizures; affected sister deceased: encephalopathy due to neuronal cytoplasmic deposit in cerebellar cortex and dentate nucleus 1 1 LOVD
00456245 Pat23 PubMed: Fernandez-Marmiesse 2014 - M - Spain - - - - - ? see paper; ... (detailed) 2 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.