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Summary Literature (4)
MIM:606176 - DIABETES MELLITUS, PERMANENT NEONATAL, 1; PNDM1

Xenbase Genes: abcc8, gck, kcnj11, ins, pdx1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019207 - DEND syndrome
MONDO:0100165 - permanent neonatal diabetes mellitus 1

Disease Ontology (DO):
DOID:0060639 - permanent neonatal diabetes mellitus