AVP mutants [extracellular region]

Stable Identifier
R-HSA-5621383
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
neurohypophyseal diabetes insipidus 12388 central diabetes insipidus, Vasopressin deficiency, vasopressin defective diabetes insipidus, Pituitary diabetes insipidus