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Summary Literature (0)
DOID:0060638 - neonatal diabetes mellitus with congenital hypothyroidism


Disease Ontology Definition: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: NDH syndrome

In OMIM:
OMIM:610199 - DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH

In Mondo Disease Ontology:
MONDO:0012436 - neonatal diabetes mellitus with congenital hypothyroidism

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : glis3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), neonatal diabetes mellitus (is_a), physical disorder (is_a)