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
01819 GSD1A storage disease, glycogen, type 1A (GSD-1A) 232200 AR 2 0 G6PC - -
00726 SCN4 neutropenia, severe congenital, type 4, autosomal recessive (SCN-4) 612541 AR 1 0 G6PC3 - -
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