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
01798 - galactokinase deficiency, cataract 230200 - 0 0 GALK1 - -
03229 NBLST-3 neuroblastoma, susceptibility to, type 3 (NBLST-3) 613014 - 0 0 ALK - -
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