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| Term | neurohypophyseal diabetes insipidus | ID (Ontology) | DOID:12388 (Human Disease) |
| Definition | 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. | ||
| Also Known As | "Pituitary diabetes insipidus" ; "vasopressin defective diabetes insipidus" ; "Vasopressin deficiency" | ||
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autosomal genetic disease |__autosomal dominant disease__ diabetes insipidus | |__central diabetes insipidus__| neurohypophyseal diabetes insipidus |
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autosomal dominant disease central diabetes insipidus |
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MESH:D020790 MIM:125700 NCI:C84933 ORDO:30925 SNOMEDCT_US_2023_03_01:267393007 UMLS_CUI:C0687720 |
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