Search Ontology:
Human Disease

neurohypophyseal diabetes insipidus

Term ID
DOID:12388
Synonyms
  • Pituitary diabetes insipidus
  • vasopressin defective diabetes insipidus
  • Vasopressin deficiency
Definition
A central diabetes insipidus that is characterized by polyuria and polydipsia due to a deficiency in vasopressin synthesis and that has_material_basis_in heterozygous mutation in the arginine vasopressin gene (AVP) on chromosome 20p13. https://pubmed.ncbi.nlm.nih.gov/15070970/
References
Ontology
Human Disease   ( DOID:12388 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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