Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
- N07.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- Short description: Heredit nephrop, NEC w diffus endocaplry prolif glomrlneph
- ICD-10-CM N07.4 is a revised 2024 ICD-10-CM code that became effective on October 1, 2023.
- This is the American ICD-10-CM version of N07.4 – other international versions of ICD-10 N07.4 may differ.
The following code(s) above N07.4 contain annotation back-references
that may be applicable to N07.4:
- N00-N99 Diseases of the genitourinary system
- N00-N08 Glomerular diseases
- N07 Hereditary nephropathy, not elsewhere classified
Approximate Synonyms
- Hereditary diffuse endocapillary proliferative glomerulonephritis
- Hereditary nephropathy
ICD-10-CM N07.4 is grouped within Diagnostic Related Group(s) (MS-DRG v41.0):
- 698 Other kidney and urinary tract diagnoses with mcc
- 699 Other kidney and urinary tract diagnoses with cc
- 700 Other kidney and urinary tract diagnoses without cc/mcc
Convert N07.4 to ICD-9-CMCode History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- 2024 (effective 10/1/2023): Revised code
- New description: Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
- 2023 description: Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
Diagnosis Index entries containing back-references to N07.4:
- NephropathyN28.9 – see also Nephritis