All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05258 CLN lipofuscinosis, ceroid, neuronal (CLN) - - 1208 1188 CLCN6, CLN3, CLN5, CLN6, CLN8, DNAJC5, MFSD8, PPT1, TPP1 - -
01649 CLN2 lipofuscinosis, ceroid, neuronal, type 2 (CLN-2) 204500 AR 12 10 TPP1 - -
04233 SCAR7 ataxia, spinocerebellar, autosomal recessive, type 7 (SCAR-7) 609270 AR 6 6 TPP1 - -
Legend   How to query  


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