All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01870 - Iminoglycinuria, digenic 242600 AR;DR - - SLC36A2, SLC6A19, SLC6A20 - -
02147 BMIQ11 body mass index quantitative trait locus 11 (BMIQ-11) 300306 - - - SLC6A14 - -
01836 HND Hartnup disorder (HND) 234500 AR - - SLC6A19 - -
01350 hyperglycinuria hyperglycinuria 138500 AD - - SLC36A2, SLC6A19, SLC6A20 - -
00139 ID intellectual disability (ID) - - 2706 2388 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
04665 MAE epilepsy, myoclonic-atonic (MAE) 616421 AD 4 5 SLC6A1 - -
04666 MRT48 mental retardation, autosomal recessive, type 48 (MRT-48) 616269 AR 1 1 SLC6A17 - -
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