Central diabetes insipidus

rare

Central diabetes insipidus (CDI) is a hypothalamus-pituitary disease characterized by polyuria and polydipsia due to a vasopressin (AVP) deficiency. It can be inherited or acquired (hereditary CDI and acquired CDI).

Identifiers: MONDO:0015790 Orphanet:178029
Part of: Neuroendocrine disorder Pituitary deficiency
Also known as: CDI · diabetes insipidus cranial type · diabetes insipidus neurogenic · diabetes insipidus neurohypophyseal · neurogenic diabetes insipidus

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Acquired central diabetes insipidus	MONDO:0019846
Neurohypophyseal diabetes insipidus	MONDO:0007450		AVP

Rare disease

Projects

Including projects on subtypes.

No projects yet.