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neurohypophyseal diabetes insipidus

Disease Summary
Associated Targets (1)
Tbio

1


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Mondo Description Hereditary central diabetes insipidus is a rare genetic subtype of central diabetes insipidus (CDI) characterized by polyuria and polydipsia due to a deficiency in vasopressin (AVP) synthesis.
Uniprot Description A disease characterized by persistent thirst, polydipsia and polyuria. Affected individuals are apparently normal at birth, but characteristically develop symptoms of vasopressin deficiency during childhood.
Mondo Term and Equivalent IDs
MONDO:0007450:  neurohypophyseal diabetes insipidus
NCIT:C84933: 
Orphanet:30925: 
SCTID:45369008: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)