N25.9
BillableDisorder rslt from impaired renal tubular function, unsp
Disorder resulting from impaired renal tubular function, unspecified
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •disorders of kidney and ureter with urolithiasisN20-N23
Related Codes(3)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(74)
SNOMED CT
- Renal tubular defect7703001
- Abnormal renal function39539005
- Renal tubular disorder95568003
- Specific renal tubule transport defect236470002
- Inherited renal tubule insufficiency with cholestatic jaundice236482006
- Renal tubule insufficiency with biliary malformation236482006
- Azotaemia445009001
- Azotemia445009001
- Azotaemia due to inadequate renal perfusion445646001
- Azotemia due to inadequate renal perfusion445646001
- Prerenal azotaemia445646001
- Prerenal azotemia445646001
- Hypertrophic mitochondrial cardiomyopathy472316006
- Renal tubulopathy with encephalopathy and liver failure syndrome717053007
- Coenzyme Q10 deficiency724575009
- Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome763280005
- Mitochondrial DNA depletion syndrome 8A encephalomyopathic type with renal tubulopathy765100000
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy765100000
- RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy765100000
- Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy765100000
- Mitochondrial DNA depletion syndrome encephalomyopathic form765401006
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form765401006
- Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation771509001
- Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation771509001
- Secondary hypertension due to renal tubular disorder1208839002
- Abnormal renal tubular function244941000119101
UMLS
- Disorder resulting from impaired renal tubular function, unspecifiedC0151747
- Disorder rslt from impaired renal tubular function, unspC0151747
- Disorder tubular kidneyC0151747
- Disorders resulting from impaired renal tubular functionC0151747
- Kidney tubular disorderC0151747
- Kidney tubule disorderC0151747
- Nephropathy tubularC0151747
- Renal tubular diseaseC0151747
- Renal tubular disorderC0151747
- Renal tubular disorder (disorder)C0151747
- Renal tubular disorder NOSC0151747
- Renal tubular dysfunctionC0151747
- renal tubular disorderC0151747
- renal tubular dysfunctionC0151747
Clinical Terms
- Nephropathy tubular
- Kidney tubule disorder
- Renal tubule insufficiency with biliary malformation
- Hypertrophic mitochondrial cardiomyopathy
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
- Secondary hypertension due to renal tubular disorder
- Specific renal tubule transport defect
- renal tubular dysfunction
- Renal tubular disorder (disorder)
- Prerenal azotemia
- Coenzyme Q10 deficiency
- Kidney tubular disorder
- Renal tubular disease
- Renal tubular disorder NOS
- RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
- Abnormal renal tubular function
- Renal tubular defect
- renal tubular disorder
- Azotemia due to inadequate renal perfusion
- Azotemia
- Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation
- Mitochondrial DNA depletion syndrome 8A encephalomyopathic type with renal tubulopathy
- Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy
- Mitochondrial DNA depletion syndrome encephalomyopathic form
- Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
- Inherited renal tubule insufficiency with cholestatic jaundice
- Disorder tubular kidney
- Abnormal renal function
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
- Prerenal azotaemia
- Azotaemia
- Azotaemia due to inadequate renal perfusion
- Renal tubulopathy with encephalopathy and liver failure syndrome
Frequently Asked Questions
What is the ICD-10 code for disorder rslt from impaired renal tubular function, unsp?
The ICD-10-CM code for disorder rslt from impaired renal tubular function, unsp is N25.9. The full clinical description is "Disorder resulting from impaired renal tubular function, unspecified". N25.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code N25.9 mean?
ICD-10-CM code N25.9 represents “Disorder resulting from impaired renal tubular function, unspecified”. It is classified under Chapter 14: Diseases of the Genitourinary System and is a billable/specific code that can be used on a claim.
Is N25.9 a billable code?
Yes, N25.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is N25.9 in?
N25.9 is in Chapter 14: Diseases of the Genitourinary System (codes N00-N99).
What SNOMED CT codes does N25.9 map to?
N25.9 maps to 16 SNOMED CT concepts: 39539005, 244941000119101, 445009001, 445646001, 724575009, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for N25.9?
N25.9 is linked to 1 UMLS Concept Unique Identifier: C0151747. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does N25.9 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorder rslt from impaired renal tubular function, unsp 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 N25.9?
N25.9 maps to the ICD-11 code: GB90.4Z (Renal tubular function disorders, unspecified).
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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.