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
03710 CLN11 lipofuscinosis, ceroid, neuronal, type 11 (CLN-11) 614706 AR - - GRN - -
03835 CMS8 myasthenic syndrome, congenital, type 8, with pre- and postsynaptic defects (CMS-8) 615120 AR 3 2 AGRN - -
02665 FTLDTDP;PPA degeneration, frontotemporal lobar, with TDP43 inclusions (FTLD-TDP, aphasia, primary progressive (PPA)) 607485 AD 8 1 GRN - -
Legend   How to query  


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