The association between AVP (Arginine Vasopressin) and Hereditary Arginine Vasopressin Deficiency is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources2
Clinical variants65
Symptoms9
Compounds0
Trials0
Publications21
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.