All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01884 - Erythrocyte lactate transporter defect 245340 AD 0 0 SLC16A1 - -
03080 CTRCT47 cataract, type 47, juvenile, with microcornea 612018 AD 0 0 SLC16A12 - -
02892 HHF7 Hyperinsulinemic hypoglycemia, familial, 7 610021 AD 0 0 SLC16A1 - -
04661 MCT1D monocarboxylate transporter 1 deficiency (MCT-1D) 616095 AD;AR 0 0 SLC16A1 - -
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