5A61.5ICD-11 MMS 2026-01
Central diabetes insipidus
Description
Central diabetes insipidus (CDI) is a hypothalamus-pituitary disease characterised by polyuria and polydipsia due to a vasopressin (AVP) deficiency. The condition may be associated with deficient secretion of antidiuretic hormone (ADH) and is most frequently idiopathic (possibly due to autoimmune injury to the ADH-producing cells), or may be induced by trauma, pituitary surgery, or hypoxic or ischaemic encephalopathy.
Index terms
- Central diabetes insipidus
- ADH - [antidiuretic hormone secretion] deficiency
- DI - [diabetes insipidus]
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- antidiuretic hormone hyposecretion
- diabetes insipidus
- diabetes insipidus secondary to vasopressin deficiency
- diabetes mellitus insipidus
- familial diabetes insipidus
- neurogenic diabetes insipidus
- primary central diabetes insipidus
- vasopressin deficiency
- vasopressin deficiency syndrome
- vasopressin hyposecretion
- Wolfram syndrome
- DIDMOAD - [Diabetes insipidus, diabetes mellitus, optic atrophy, and deafness] syndrome
- Diabetes insipidus, diabetes mellitus, optic atrophy, and deafness
- Acquired central diabetes insipidus
- Acquired central diabetes due to Infiltrative disease
- Idiopathic acquired central diabetes insipidus
- Traumatic central diabetes insipidus
- Non-acquired central diabetes insipidus
- Cranial diabetes insipidus
- Neurohypophyseal diabetes insipidus
Inclusions
- ADH - [antidiuretic hormone secretion] deficiency
Excludes
GB90.4A– Nephrogenic diabetes insipidus
Exclusions from above levels
2A00– Craniopharyngioma5D43– Postprocedural hypopituitarism18– Pregnancy, childbirth or the puerperium
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- http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn
Sibling codes
Foundation entity
Central diabetes insipidus – http://id.who.int/icd/entity/1009553897
Part of: 5A61: Hypofunction or certain other specified disorders of pituitary gland › 05: Endocrine, nutritional or metabolic diseases