Effective from
- Added
Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]
Billable diagnosis code
CDC/NCHS · FY2026hypertensive chronic kidney disease (I12.-)
Coverage depends on the payer, service and applicable policy. A billable code does not guarantee payment.
For US diagnosis claims covered by HIPAA, ICD-10-CM is required from October 1, 2015.
Use the service date for outpatient/professional claims and the discharge date for hospital inpatient claims. Earlier encounters use ICD-9-CM; each individual code must also be valid for the applicable date.
Official coding guidelines → · CMS ↗First observed · 2025-10-01
Latest recorded change · FY2026
Effective from
Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]
Billable diagnosis code
CDC/NCHS · FY2026| All editions | Effective from | Code history |
|---|---|---|
| FY2026 | 2025-10-01 | Added |
| FY2026 · April | 2026-04-01 | No tabular change |
| FY2027 | 2026-10-01 | No tabular change |
hypertensive chronic kidney disease (I12.-)
Historical assignments from the CDC conversion table support data retrieval. They do not authorize substituting a previous code for the current code.
Previous assignment: N07.8
Other entries in the same category; these are not automatic substitutes.
| Code | Description | Category · further specificity required |
|---|---|---|
| N07.0 | Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality | Billable / specific |
| N07.1 | Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions | Billable / specific |
| N07.2 | Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis | Billable / specific |
| N07.3 | Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis | Billable / specific |
| N07.4 | Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis | Billable / specific |
| N07.5 | Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis | Billable / specific |
| N07.6 | Hereditary nephropathy, not elsewhere classified with dense deposit disease | Billable / specific |
| N07.7 | Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis | Billable / specific |
| N07.8 | Hereditary nephropathy, not elsewhere classified with other morphologic lesions | Billable / specific |
| N07.9 | Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions | Billable / specific |
| N07.A | Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis | Billable / specific |
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