AVPR2

arginine vasopressin receptor 2
OMIM: 300538
PanelMode of inheritanceDetails
1 panel
R-numbers: R198
Signed-off version 3.1
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Diabetes insipidus, nephrogenic, OMIM:304800, Nephrogenic syndrome of inappropriate antidiuresis, OMIM:300539