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neonatal diabetes mellitus with congenital hypothyroidism (DOID:0060638)
Alliance: disease page
Synonyms: NDH syndrome
Alt IDs: OMIM:610199, ORDO:79118
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.

Disease References using Mouse Models (3)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
06/15/2021
MGI 6.17 		The Jackson Laboratory