|
General Information
|
| Term |
neonatal diabetes mellitus with congenital hypothyroidism |
ID (Ontology) |
DOID:0060638 (Human Disease) |
| 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. |
| Also Known As |
"NDH syndrome" |
| Comment |
|
|
Links to External Ontologies
|
|
DO.org
|
|
Annotations
|
|
Records annotated with this term OR any of its CHILD TERMS
|
|
|
|
Records annotated with this exact term (annotations to child terms are NOT included)
|
|
No relevant records available
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Genes |
|---|
neonatal diabetes mellitus with congenital hypothyroidism | 1 | for disease ribbon | neonatal diabetes mellitus with congenital hypothyroidism | 1 | model of | neonatal diabetes mellitus with congenital hypothyroidism | 1 |
|
Relationships