N25.1
BillableNephrogenic diabetes insipidus
Nephrogenic diabetes insipidus
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- diabetes insipidus NOS (E23.2)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- disorders of kidney and ureter with urolithiasis (N20-N23)
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
- Acquired AVP (arginine vasopressin) resistance81475007
- Acquired AVP-R (arginine vasopressin resistance)81475007
- Acquired nephrogenic diabetes insipidus81475007
- Acquired vasopressin resistance81475007
- AVP-R - arginine vasopressin resistance111395007
- Arginine vasopressin resistance111395007
- NDI - Nephrogenic diabetes insipidus111395007
- Nephrogenic diabetes insipidus111395007
- Vasopressin resistance111395007
- Arginine vasopressin resistance, intracranial calcification, short stature, facial dysmorphism syndrome716200002
- Nephrogenic diabetes insipidus and intracranial calcification syndrome716200002
- Schofer Beetz Bohl syndrome716200002
- Autosomal hereditary AVP-R (arginine vasopressin resistance)1296897006
- Autosomal hereditary arginine vasopressin resistance1296897006
- Autosomal hereditary vasopressin resistance1296897006
- Hereditary nephrogenic diabetes insipidus1296897006
- Hereditary AVP-R (arginine vasopressin resistance)1296898001
- Hereditary arginine vasopressin resistance1296898001
- Hereditary vasopressin resistance1296898001
- Autosomal dominant hereditary AVP-R (arginine vasopressin resistance)1296908006
- Autosomal dominant hereditary arginine vasopressin resistance1296908006
- Autosomal dominant hereditary vasopressin resistance1296908006
- Autosomal dominant vasopressin resistance1296908006
- Autosomal recessive hereditary AVP-R (arginine vasopressin resistance)1296909003
- Autosomal recessive hereditary arginine vasopressin resistance1296909003
- Autosomal recessive hereditary vasopressin resistance1296909003
- Autosomal recessive vasopressin resistance1296909003
- X-linked hereditary AVP-R (arginine vasopressin resistance)1296910008
- X-linked hereditary arginine vasopressin resistance1296910008
- X-linked hereditary vasopressin resistance1296910008
- Hereditary AVP (arginine vasopressin)-related polyuria1296911007
- Hereditary arginine vasopressin-related polyuria1296911007
- Hereditary vasopressin-related polyuria1296911007
- Secondary AVP-R (arginine vasopressin resistance)1296921004
- Secondary arginine vasopressin resistance1296921004
- Secondary vasopressin resistance1296921004
- Partial AVP (arginine vasopressin)-related polyuria68061000119109
- Partial arginine vasopressin-related polyuria68061000119109
- Partial diabetes insipidus68061000119109
- Partial vasopressin-related polyuria68061000119109
- Partial AVP-R (arginine vasopressin resistance)368961000119107
- Partial arginine vasopressin resistance368961000119107
- Partial nephrogenic diabetes insipidus368961000119107
- Partial vasopressin resistance368961000119107
UMLS
- AVP-R - arginine vasopressin resistanceC0162283
- Arginine vasopressin resistanceC0162283
- Arginine vasopressin resistance (disorder)C0162283
- Diabetes Insipidus, NephrogenicC0162283
- Diabetes insipidus nephrogenicC0162283
- Diabetes insipidus, nephrogenicC0162283
- NDIC0162283
- NDI - Nephrogenic diabetes insipidusC0162283
- Nephrogenic Diabetes InsipidusC0162283
- Nephrogenic diabetes insipidusC0162283
- Vasopressin resistanceC0162283
- diabete insipidus nephrogenicC0162283
- diabetes insipidus nephrogenicC0162283
- nephrogenic diabetes insipidusC0162283
Frequently Asked Questions
What is ICD-10 code N25.1?
ICD-10-CM code N25.1 represents "Nephrogenic diabetes insipidus". It is a billable/specific code that can be used on a claim.
Is N25.1 a billable code?
Yes, N25.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is N25.1 in?
N25.1 is in Chapter 14: Diseases of the Genitourinary System (codes N00-N99).
What codes cannot be used with N25.1?
N25.1 has Excludes1 notes indicating codes that cannot be used together with it, including: diabetes insipidus NOS (E23.2).
What SNOMED CT codes does N25.1 map to?
N25.1 maps to 13 SNOMED CT concepts: 111395007, 81475007, 716200002, 1296908006, 1296897006, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for N25.1?
N25.1 is linked to 1 UMLS Concept Unique Identifier: C0162283. 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.