AutoICD API

E23.2

Billable

Diabetes insipidus

Diabetes insipidus

Status

Billable / Specific

Block

E20-E35

Parent Code

E23

ICD-11 Mapping

1 equivalent

Coding Notes

Includes

Conditions included under this code

  • the listed conditions whether the disorder is in the pituitary or the hypothalamus

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Related Codes(5)
E23.0

Hypopituitarism

BillableE23.1

Drug-induced hypopituitarism

BillableE23.3

Hypothalamic dysfunction, not elsewhere classified

BillableE23.6

Other disorders of pituitary gland

BillableE23.7

Disorder of pituitary gland, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

5A61.5Central diabetes insipidusequivalentPrimary
Also Known As / Clinical Terms(243)

SNOMED CT

UMLS

Clinical Terms

  • Arginine vasopressin deficiency due to trauma
  • Weakness of both lower limbs
  • Wolfram syndrome type I
  • Muscle weakness of all four limbs
  • Diabetes insipidus - pituitary
  • Familial vasopressin deficiency
  • Autosomal recessive hereditary AVP-D (arginine vasopressin deficiency)
  • Hypohidrosis-diabetes insipidus syndrome
  • Vasopressin deficiency
  • AVP-D - arginine vasopressin deficiency
  • Paresis of left lower limb
  • Marquardt-Loriaux syndrome
  • Leber's amaurosis
  • Familial vasopressin-related polyuria
  • Secondary vasopressin-related polyuria
  • Weakness of left upper limb
  • Neurohypophyseal diabetes insipidus
  • Always thirsty
  • WFS1 - Wolfram syndrome-1
  • Secondary diabetes insipidus
  • AVP (arginine vasopressin)-related polyuria
  • Partial vasopressin-related polyuria
  • Post-traumatic vasopressin deficiency
  • X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome
  • Quadriparesis
  • Idiopathic vasopressin-related polyuria
  • Bilateral optic atrophy of eyes
  • Familial AVP (arginine vasopressin)-related polyuria
  • Familial central diabetes insipidus
  • Autosomal recessive hereditary vasopressin deficiency
  • Late effect of traumatic injury to brain
  • Optic atrophy of both eyes
  • Secondary AVP (arginine vasopressin)-related polyuria
  • AVP-D (arginine vasopressin deficiency) due to trauma
  • Vasopressin deficiency due to trauma
  • CRB - Congenital retinal blindness
  • Autosomal recessive hereditary arginine vasopressin deficiency
  • diabete insipidus
  • DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) syndrome
  • Wolfram syndrome type 1
  • Hereditary AVP (arginine vasopressin)-related polyuria
  • Spastic quadriparesis
  • Weakness of left lower limb
  • Adipsic vasopressin-related polyuria
  • Post-traumatic central diabetes insipidus
  • Paresis of right lower extremity
  • WFS2 - Wolfram syndrome-2
  • Optic atrophy of bilateral eyes
  • Wolfram syndrome type 2
  • Excessive thirst
  • Late effect of brain injury
  • Secondary arginine vasopressin-related polyuria
  • Wolfram syndrome
  • Partial arginine vasopressin-related polyuria
  • Arginine vasopressin-related polyuria
  • Arginine vasopressin deficiency
  • Partial AVP (arginine vasopressin)-related polyuria
  • Dipsogenic diabetes insipidus
  • Partial diabetes insipidus
  • Arginine vasopressin-related polyuria (disorder)
  • weakness of left arm
  • Hereditary arginine vasopressin-related polyuria
  • Primary polydipsia
  • Paresis of left lower extremity
  • Wolfram syndrome type II
  • Congenital retinal blindness
  • Weakness of both legs
  • Postoperative central diabetes insipidus
  • Weakness of right arm
  • Familial arginine vasopressin deficiency
  • Oligohidrosis
  • Fleck syndrome
  • Postoperative vasopressin deficiency
  • Spastic tetraparesis
  • Weakness of right upper limb
  • Familial AVP-D (arginine vasopressin deficiency)
  • Hereditary vasopressin-related polyuria
  • Weakness of left leg
  • Postoperative cranial diabetes insipidus
  • Paresis of right lower limb
  • Weakness of both lower extremities
  • Postoperative neurohypophyseal diabetes insipidus
  • Pituitary diabetes insipidus
  • Tetraparesis
  • Desperate to drink
  • Leber amaurosis
  • Postoperative arginine vasopressin deficiency
  • Weakness of bilateral lower limb
  • Idiopathic diabetes insipidus
  • Familial arginine vasopressin-related polyuria
  • Leber congenital amaurosis
  • Keen for fluids
  • Weakness of bilateral lower extremities
  • Idiopathic arginine vasopressin-related polyuria
  • Autosomal dominant hereditary vasopressin deficiency
  • Delayed onset arginine vasopressin deficiency due to and following traumatic brain injury
  • Secondary arginine vasopressin deficiency
  • Weakness of right lower limb
  • Central diabetes insipidus
  • Autosomal dominant hereditary arginine vasopressin deficiency
  • Idiopathic AVP (arginine vasopressin)-related polyuria
  • Hypohydrosis
  • Adipsic AVP (arginine vasopressin)-related polyuria
  • Neurogenic diabetes insipidus
  • Familial diabetes insipidus
  • DIDMOAD syndrome
  • Autosomal dominant hereditary AVP-D (arginine vasopressin deficiency)
  • Hypohidrosis
  • Bilateral weakness of legs
  • Central diabetes insipidus due to and following traumatic event
  • Weakness of right leg
  • Secondary AVP-D (arginine vasopressin deficiency)
  • Postoperative AVP-D (arginine vasopressin deficiency)
  • Secondary vasopressin deficiency
  • Cranial diabetes insipidus
  • Adipsic arginine vasopressin-related polyuria
  • X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency
  • Vasopressin-related polyuria
Frequently Asked Questions
What is the ICD-10 code for diabetes insipidus?

The ICD-10-CM code for diabetes insipidus is E23.2. The full clinical description is "Diabetes insipidus". E23.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E23.2 mean?

ICD-10-CM code E23.2 represents “Diabetes insipidus”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E23.2 a billable code?

Yes, E23.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E23.2 in?

E23.2 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E23.2?

E23.2 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 3 more.

What SNOMED CT codes does E23.2 map to?

E23.2 maps to 35 SNOMED CT concepts: 1296758008, 1186863001, 45369008, 1297073009, 17173007, and 30 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E23.2?

E23.2 is linked to 1 UMLS Concept Unique Identifier: C0011848. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E23.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like diabetes insipidus affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E23.2?

E23.2 maps to the ICD-11 code: 5A61.5 (Central diabetes insipidus).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.