All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00063 HHF1 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1 256450 AD;AR - - ABCC8 - -
00064 LIH HYPOGLYCEMIA, LEUCINE-INDUCED 240800 AD - - ABCC8 - -
00061 PNDM3 DIABETES MELLITUS, PERMANENT NEONATAL, 3 618857 AD;AR - - ABCC8 - -
00051 T2D TYPE 2 DIABETES MELLITUS 125853 AD - - ABCC8, GCK, HNF1A, HNF4A, NEUROD1, PAX4 - -
00062 TNDM2 DIABETES MELLITUS, TRANSIENT NEONATAL, 2 610374 - - - ABCC8 - -
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