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Echinobase
Summary Literature (0)
DOID:0060639 - permanent neonatal diabetes mellitus

Disease Ontology Definition:A neonatal diabetes mellitus that has_material_basis_in homozygous mutation in the glucokinase gene (GCK), heterozygous mutation in the KCNJ11 and INS genes, or by heterozygous or homozygous mutation in the ABCC8 gene.

Synonyms: PDMI, PNDM, permanent diabetes mellitus of infancy,

Echinobase Genes : gck


OMIM:
MIM:606176 - diabetes mellitus, permanent neonatal; pndm

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): neonatal diabetes mellitus (is_a)