FY2016
Effective from
- First observed
Hereditary nephropathy, not elsewhere classified
Category — select a more specific code
CDC/NCHS · FY2016hypertensive chronic kidney disease (I12.-)
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 · 2015-10-01
No recorded change since first observation
Effective from
Hereditary nephropathy, not elsewhere classified
Category — select a more specific code
CDC/NCHS · FY2016| All editions | Effective from | Code history |
|---|---|---|
| FY2016 | 2015-10-01 | First observed |
| FY2017 | 2016-10-01 | No tabular change |
| FY2018 | 2017-10-01 | No tabular change |
| FY2019 | 2018-10-01 | No tabular change |
| FY2020 | 2019-10-01 | No tabular change |
| FY2020 · April | 2020-04-01 | No tabular change |
| FY2021 | 2020-10-01 | No tabular change |
| FY2021 · 01-01 | 2021-01-01 | No tabular change |
| FY2022 | 2021-10-01 | No tabular change |
| FY2022 · 04-01 | 2022-04-01 | No tabular change |
| FY2023 | 2022-10-01 | No tabular change |
| FY2023 · 04-01 | 2023-04-01 | No tabular change |
| FY2024 | 2023-10-01 | No tabular change |
| FY2024 · 04-01 | 2024-04-01 | No tabular change |
| FY2025 | 2024-10-01 | No tabular change |
| FY2025 · 04-01 | 2025-04-01 | No tabular change |
| FY2026 | 2025-10-01 | No tabular change |
| FY2026 · April | 2026-04-01 | No tabular change |
| FY2027 | 2026-10-01 | No tabular change |
hypertensive chronic kidney disease (I12.-)
N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormalityBillable / specificN07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesionsBillable / specificN07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritisBillable / specificN07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritisBillable / specificN07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritisBillable / specificN07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritisBillable / specificN07.6Hereditary nephropathy, not elsewhere classified with dense deposit diseaseBillable / specificN07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritisBillable / specificN07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesionsBillable / specificN07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesionsBillable / specificN07.AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritisBillable / specificN07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]Billable / specificOfficial titles and instructions are preserved in their source language. Official sources ↗