All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00021 MSA Multiple System Atrophy 146500 - 26 - COQ2, POLG - -
00025 NCL Neuronal Ceroid-Lipofuscinoses 256370 - 392 - CLCN6, CLN3, CLN5, CLN6, CLN8, CTSD, MFSD8, POLG, PPT1, SGSH, TPP1 - -
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