Human genes for neurohypophyseal diabetes insipidus
Neurohypophyseal diabetes insipidus [DOID:12388]
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: neurohypophyseal diabetes insipidus, DOID:12388, neurohypophyseal diabetes insipiduses, neurohypophyseal diabetes insipidi, Pituitary diabetes insipidus ...