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
04631 NLS-2 Neu-Laxova syndrome, tyep 2 (NLS-2) 616038 - 13 13 PSAT1 - -
03002 PSATD deficiency, phosphoserine aminotransferase (PSATD) 610992 - 2 2 PSAT1 - -
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