DISEASES

Disease-gene associations mined from literature

Human genes for neonatal diabetes mellitus with congenital hypothyroidism

Neonatal diabetes mellitus with congenital hypothyroidism [DOID:0060638]

A neonatal diabetes that is characterized by intrauterine growth retardation, hypothyroidism and onset of nonimmune diabetes mellitus within the first few weeks of life, and that has_material_basis_in homozygous or compound heterozygous mutations in the GLIS3 gene on chromosome 9p24.

Synonyms:  neonatal diabetes mellitus with congenital hypothyroidism,  DOID:0060638,  neonatal diabetes mellitus with congenital hypothyroidisms,  NDH syndrome,  NDH disease ...