neonatal diabetes mellitus with congenital hypothyroidism

Summary

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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: glis3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012436 - neonatal diabetes mellitus with congenital hypothyroidism

MONDO:0012436 - neonatal diabetes mellitus with congenital hypothyroidism

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), inherited metabolic disorder (is_a), neonatal diabetes (is_a), physical disorder (is_a)