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DO Term : neonatal diabetes mellitus with congenital hypothyroidism [DOID:0060638] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • 610199,
  • OMIM:610199,
  • NDH syndrome,
  • ORDO:79118
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents