E23.2
BillableDiabetes insipidus
Diabetes insipidus
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)
Also Known As / Clinical Terms
SNOMED CT
- Secondary AVP (arginine vasopressin)-related polyuria13196008
- Secondary arginine vasopressin-related polyuria13196008
- Secondary diabetes insipidus13196008
- Secondary vasopressin-related polyuria13196008
- Always thirsty17173007
- Desperate to drink17173007
- Excessive thirst17173007
- Keen for fluids17173007
- Familial AVP (arginine vasopressin)-related polyuria42021008
- Familial arginine vasopressin-related polyuria42021008
- Familial diabetes insipidus42021008
- Familial vasopressin-related polyuria42021008
- Hypohidrosis45004005
- Hypohydrosis45004005
- Oligohidrosis45004005
- AVP-D - arginine vasopressin deficiency45369008
- Arginine vasopressin deficiency45369008
- Central diabetes insipidus45369008
- Cranial diabetes insipidus45369008
- Diabetes insipidus - pituitary45369008
- Neurogenic diabetes insipidus45369008
- Neurohypophyseal diabetes insipidus45369008
- Pituitary diabetes insipidus45369008
- Vasopressin deficiency45369008
- DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) syndrome70694009
- DIDMOAD syndrome70694009
- Marquardt-Loriaux syndrome70694009
- Wolfram syndrome70694009
- Idiopathic AVP (arginine vasopressin)-related polyuria77274005
- Idiopathic arginine vasopressin-related polyuria77274005
- Idiopathic diabetes insipidus77274005
- Idiopathic vasopressin-related polyuria77274005
- Dipsogenic diabetes insipidus82800008
- Primary polydipsia82800008
- Muscle weakness of all four limbs91327001
- Quadriparesis91327001
- Tetraparesis91327001
- CRB - Congenital retinal blindness193413001
- Congenital retinal blindness193413001
- Leber amaurosis193413001
- Leber congenital amaurosis193413001
- Leber's amaurosis193413001
- Familial AVP-D (arginine vasopressin deficiency)237696003
- Familial arginine vasopressin deficiency237696003
- Familial central diabetes insipidus237696003
- Familial vasopressin deficiency237696003
- Fleck syndrome239026002
- Hypohidrosis-diabetes insipidus syndrome239026002
- Spastic quadriparesis298282001
- Spastic tetraparesis298282001
- Late effect of brain injury429656004
- Late effect of traumatic injury to brain429656004
- X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency732246009
- X-linked intellectual disability, limb spasticity, retinal dystrophy, diabetes insipidus syndrome732246009
- Postoperative AVP-D (arginine vasopressin deficiency)1148694009
- Postoperative arginine vasopressin deficiency1148694009
- Postoperative central diabetes insipidus1148694009
- Postoperative cranial diabetes insipidus1148694009
- Postoperative neurohypophyseal diabetes insipidus1148694009
- Postoperative vasopressin deficiency1148694009
- AVP-D (arginine vasopressin deficiency) due to trauma1186863001
- Arginine vasopressin deficiency due to trauma1186863001
- Central diabetes insipidus due to and following traumatic event1186863001
- Post-traumatic central diabetes insipidus1186863001
- Post-traumatic vasopressin deficiency1186863001
- Vasopressin deficiency due to trauma1186863001
- WFS1 - Wolfram syndrome-11285518004
- Wolfram syndrome type 11285518004
- Wolfram syndrome type I1285518004
- WFS2 - Wolfram syndrome-21285519007
- Wolfram syndrome type 21285519007
- Wolfram syndrome type II1285519007
- AVP (arginine vasopressin)-related polyuria1296758008
- Arginine vasopressin-related polyuria1296758008
- Diabetes insipidus1296758008
- Vasopressin-related polyuria1296758008
- Hereditary AVP (arginine vasopressin)-related polyuria1296911007
- Hereditary arginine vasopressin-related polyuria1296911007
- Hereditary vasopressin-related polyuria1296911007
- Autosomal dominant hereditary AVP-D (arginine vasopressin deficiency)1296914004
- Autosomal dominant hereditary arginine vasopressin deficiency1296914004
- Autosomal dominant hereditary vasopressin deficiency1296914004
- Autosomal recessive hereditary AVP-D (arginine vasopressin deficiency)1296915003
- Autosomal recessive hereditary arginine vasopressin deficiency1296915003
- Autosomal recessive hereditary vasopressin deficiency1296915003
- Secondary AVP-D (arginine vasopressin deficiency)1296920003
- Secondary arginine vasopressin deficiency1296920003
- Secondary vasopressin deficiency1296920003
- Adipsic AVP (arginine vasopressin)-related polyuria1297073009
- Adipsic arginine vasopressin-related polyuria1297073009
- Adipsic vasopressin-related polyuria1297073009
- Delayed onset arginine vasopressin deficiency due to and following traumatic brain injury1365942003
- Bilateral optic atrophy of eyes15632891000119109
- Optic atrophy of bilateral eyes15632891000119109
- Optic atrophy of both eyes15632891000119109
- Bilateral weakness of legs691011000124106
- Weakness of bilateral lower extremities691011000124106
- Weakness of bilateral lower limb691011000124106
- Weakness of both legs691011000124106
- Weakness of both lower extremities691011000124106
- Weakness of both lower limbs691011000124106
- Paresis of left lower extremity16018391000119104
- Paresis of left lower limb16018391000119104
- Paresis of right lower extremity16018431000119109
- Paresis of right lower limb16018431000119109
- Partial AVP (arginine vasopressin)-related polyuria68061000119109
- Partial arginine vasopressin-related polyuria68061000119109
- Partial diabetes insipidus68061000119109
- Partial vasopressin-related polyuria68061000119109
- Weakness of left leg570941000124100
- Weakness of left lower limb570941000124100
- Weakness of left upper limb570921000124107
- weakness of left arm570921000124107
- Weakness of right arm570961000124101
- Weakness of right upper limb570961000124101
- Weakness of right leg570971000124108
- Weakness of right lower limb570971000124108
Frequently Asked Questions
What is ICD-10 code E23.2?
ICD-10-CM code E23.2 represents "Diabetes insipidus". It 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.
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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.