Diabetes Insipidus, Neurogenic
Disease ID: disease_node_10720
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| Dbxref | MESH:D020790, MIM:125700, NCI:C84933, ORDO:30925, SNOMEDCT_US_2023_03_01:267393007, UMLS_CUI:C0687720 |
|---|---|
| Subclassof | DOID_0050736, DOID_0081055 |
| Data Source | DOID, MESH |
| Synonyms | Pituitary diabetes insipidus, Vasopressin deficiency, vasopressin defective diabetes insipidus |
| Mesh Id | D020790 |
| Mesh Label | Diabetes Insipidus, Neurogenic |
| Mesh Subclassof | D003919 |
| Doid Label | neurohypophyseal diabetes insipidus |
| Doid Description | A central diabetes insipidus that is characterized by polyuria and polydipsia due to a deficiency in vasopressin synthesis and that has_material_basis_in heterozygous mutation in the arginine vasopressin gene (AVP) on chromosome 20p13. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_10720 |
| Doid Id | DOID_12388 |
| Label | Diabetes Insipidus, Neurogenic |
- Outgoing r'ship
SUBCLASS_OFto/from Central Diabetes Insipidus(ID:disease_node_19684) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)