has material basis in germline mutation in disease has location AVP autosomal dominant disease pituitary gland disorder diabetes insipidus neurohypophyseal diabetes insipidus https://www.malacards.org/card/diabetes_insipidus_neurohypophyseal https://www.malacards.org/card/hereditary_arginine_vasopressin_deficiency AVP deficiency MEDGEN:574999 SCTID:45369008 DOID:12388 ADH deficiency icd11.foundation:97299603 GARD:0016629 UMLS:C0342394 NANDO:2201050 hereditary CDI NCIT:C84933 Orphanet:30925 hereditary neurogenic diabetes insipidus Arginine vasopressin deficiency vasopressin deficiency antidiuretic hormone deficiency pituitary gland diabetes insipidus MONDO:0007450 diabetes insipidus of pituitary gland Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis. OMIM:125700 central diabetes insipidus inherited kidney disorder hereditary neurological disease pituitary gland