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Summary Literature (0)
DOID:12388 - neurohypophyseal diabetes insipidus

Disease Ontology 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.

Synonyms: central diabetes insipidus, Pituitary diabetes insipidus, vasopressin defective diabetes insipidus, Vasopressin deficiency

Xenbase Genes : avp

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007450 - neurohypophyseal diabetes insipidus


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), central diabetes insipidus (is_a), pancreas disease (is_a)