Search Ontology:
Human Disease

neonatal diabetes mellitus with congenital hypothyroidism

Term ID
DOID:0060638
Synonyms
  • NDH syndrome
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. https://www.ncbi.nlm.nih.gov/pubmed/16715098
References
Ontology
Human Disease   ( DOID:0060638 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations