Term Name: neurohypophyseal diabetes insipidus
Synonyms: Pituitary diabetes insipidus, vasopressin defective diabetes insipidus, Vasopressin deficiency
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.
Ontology: Human Disease [DOID:12388]   ( DOID:12388 )

Relationships
is a type of: autosomal dominant disease central diabetes insipidus