Disease-gene associations mined from literature

Human genes for neonatal diabetes mellitus

Neonatal diabetes mellitus [DOID:11717]

A genetic disease that is characterized by slow growth before and after birth, intellectual disability that is usually severe to profound, skeletal abnormalities involving the arms and hands, and distinctive facial features.

Synonyms:  neonatal diabetes mellitus,  DOID:11717,  diabetes mellitus syndrome in newborn infant

Linkouts:  OMIM #1 #2 #3 #4