AVP mutants [extracellular region]

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