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DOID:0060638 - neonatal diabetes mellitus with congenital hypothyroidism
Disease Ontology Definition:A neonatal diabetes mellitus characterized by intrauterine growth retardation, hypothyroidism and onset of nonimmune diabetes mellitus within the first few weeks of life; it has_material_basis_in homozygous or compound heterozygous mutations in the GLIS3 gene on chromosome 9p24.
Synonyms: NDH syndrome,
Echinobase Genes
:
glis3
| MIM:610199 - diabetes mellitus, neonatal, with congenital hypothyroidism |
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)