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
01870 - Iminoglycinuria 242600 - 0 0 SLC36A2, SLC6A19, SLC6A20 - -
01350 hyperglycinuria hyperglycinuria 138500 AD 0 0 SLC36A2, SLC6A19, SLC6A20 - -
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