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	-
Date created	2020-03-03 14:34:43 +00:00 (UTC)
Date last edited	2023-06-16 09:21:50 +00:00 (UTC)

MVZ für Humangenetik Regensburg