N07.3
N07.3: Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
Billable / specific codeICD-10-CM
N07.3 is a billable, specific ICD-10-CM code for hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis. It is valid for submission on a claim.
Check N07.3 with the rest of the claim: free scrubberExcludes2 inherited from the categories above N07.3
Not part of this code, but both may be coded when both are present.
Risk adjustment
No CMS-HCC V28 category: this code does not change a RAF score.
Medicare coverage
N07.3 is named in 2 Medicare coverage policies: 2 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A55336Billing and Coding: Retroperitoneal Ultrasound
- A57189Billing and Coding: Serum Magnesium
Alphabetic index entries that lead here
- Nephropathy›hereditary NEC›with›diffuse›mesangial proliferative glomerulonephritis
Code history
Unchanged in every release from FY2024 to FY2027.
Other codes under N07
- N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
- N07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
- N07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
- N07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
- N07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
- N07.6Hereditary nephropathy, not elsewhere classified with dense deposit disease
- N07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
- N07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesions
- N07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
- N07.AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
- N07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]