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Disease Ontology Browser
neurohypophyseal diabetes insipidus (DOID:12388)
Alliance: disease page
Synonyms: Pituitary diabetes insipidus; vasopressin defective diabetes insipidus; Vasopressin deficiency
Alt IDs: OMIM:125700, MESH:D020790, NCI:C84933, ORDO:30925, UMLS_CUI:C0687720
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.

Disease References using Mouse Models (4)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory