Disease #00051 (T2D (TYPE 2 DIABETES MELLITUS), OMIM:125853)

Official abbreviation T2D
Name TYPE 2 DIABETES MELLITUS
OMIM ID 125853
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 6 genes ABCC8, GCK, HNF1A, HNF4A, NEUROD1, PAX4
Associated tissues -
Disease features -
Remarks -