Neonatal Diabetes Mellitus With Congenital Hypothyroidism
Disease ID: disease_node_17246
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:610199, ORDO:79118 |
|---|---|
| Subclassof | DOID_0080015, DOID_11717, DOID_0050737 |
| Data Source | DOID |
| Synonyms | NDH syndrome |
| Doid Label | neonatal diabetes mellitus with congenital hypothyroidism |
| Doid 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. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17246 |
| Doid Id | DOID_0060638 |
| Disease Has Basis In | HP_0001197 |
| Label | Neonatal Diabetes Mellitus With Congenital Hypothyroidism |
- Outgoing r'ship
SUBCLASS_OFto/from Neonatal Diabetes(ID:disease_node_17244) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease)