All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03710 CLN-11 lipofuscinosis, ceroid, neuronal, type 11 (CLN-11) 614706 - 0 0 GRN - -
03835 CMS-8 myasthenic syndrome, congenital, type 8, with pre- and postsynaptic defects (CMS-8) 615120 - 1 1 AGRN - -
02665 FTLD-TDP;PPA degeneration, frontotemporal lobar, with TDP43 inclusions (FTLD-TDP, aphasia, primary progressive (PPA)) 607485 - 8 1 GRN - -
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