All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01350 - Hyperglycinuria 138500 - 0 0 SLC36A2, SLC6A19, SLC6A20 - -
01870 - Iminoglycinuria 242600 - 0 0 SLC36A2, SLC6A19, SLC6A20 - -
02147 BMIQ-11 body mass index quantitative trait locus 11 (BMIQ-11) 300306 - 0 0 SLC6A14 - -
01836 HND Hartnup disorder (HND) 234500 - 0 0 SLC6A19 - -
04665 MAE epilepsy, myoclonic-atonic (MAE) 616421 - 0 0 SLC6A1 - -
04666 MRT-48 mental retardation, autosomal recessive, type 48 (MRT-48) 616269 - 0 0 SLC6A17 - -
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