Mondo Description Any maturity-onset diabetes of the young in which the cause of the disease is a mutation in the INS gene.

Uniprot Description A form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age), a primary defect in insulin secretion and frequent insulin-independence at the beginning of the disease.

Disease Ontology Description A maturity-onset diabetes of the young that has_material_basis_in heterozygous mutation in the INS gene on chromosome 11p15.5.