Neonatal diabetes (activating mutations in KCNJ11 adn ABCC8, encoding Kir6.2 and SUR1, respectively
Maternally inherited diabetes and deafness (MIDD) due to mitochondrial DNA mutations (m.3243→G)
Defects in proinsulin conversion
Insulin gene mutation
Genetic defects in insulin action
Type A insulin resistance
Lipoatrophic diabetes
Exocrine pancreatic defects
Chronic pancreatitis
Pancreatectomy/trauma
Neoplasia
Cystic fibrosis
Hemochromatosis
Fibrocalculous pancreatopathy
Endocrinopathies
Acromegaly
Cushing syndrome
Hyperthyroidism
Pheochromocytoma
Glucagonoma
Infections
Cytomegalovirus
Coxsackie B virus
Congenital rubella
Drugs
Glucocorticoids
Thyroid hormone
Interferon – α
Protease inhibitors
β- Adrenergic agonists
Thiazides
Nicotinic acid
Phenytoin
Vacor
Genetic syndromes associated with diabetes
Downs syndrome
Klinefelter syndrome
Turner syndrome
Prader-Willi syndrome
Gestational diabetes mellitus
Reference
American Diabetes Association: Position statement from the American Diabetes Association on the diagnosis and classification of diabetes mellitus. Diabetes Care 31 (Suppl. 1):S55-S60,2008
Anirban Maitra. The Endocrine system.In: Robbins and Cotran Pathologic basis of disease.9th edition.volume II.chapter 24. pp 1073-1141.