ICD-10-CM › N00-N99 › N00-N08 › N07 Hereditary nephropathy, not... › N07.4
Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
ValidICD-10-CM diagnosis code.
Valid for claims with a date of service in the current code year.
What has happened to this code
Every change the publisher made, from 2007 to now. Entries marked draft are from the pre-implementation releases: ICD-10 took effect on 1 October 2015, so nothing before FY2016 was ever valid on a claim.
- FY2007 Added to the draft code set draft Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
Official coding rules
Published by CDC for FY2027. A rule attached to a category binds every code beneath it, so the rules inherited from this code's ancestors are shown with the code they come from.
Inherited from N07 Hereditary nephropathy, not elsewhere classified
Excludes2 - not included here
- Alport's syndrome (Q87.81-)
- hereditary amyloid nephropathy (E85.-)
- nail patella syndrome (Q87.2)
- non-neuropathic heredofamilial amyloidosis (E85.-)
Inherited from the N00-N08 section Glomerular diseases (N00-N08)
Excludes1 - never coded here
- hypertensive chronic kidney disease (I12.-)
Code also
- any associated kidney failure (N17-N19).
How CDC's index refers to this code
Wording from the official alphabetic index. Much of it appears nowhere in the code description, which is why a search for the everyday phrase so often finds nothing.
- Nephropathy > hereditary NEC > with > diffuse > endocapillary proliferative glomerulonephritis
Codes in the same group
| Code | Description | Status |
|---|---|---|
| N07.0 | Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality | Valid |
| N07.1 | Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions | Valid |
| N07.2 | Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis | Valid |
| N07.3 | Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis | Valid |
| N07.5 | Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis | Valid |
| N07.6 | Hereditary nephropathy, not elsewhere classified with dense deposit disease | Valid |
| N07.7 | Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis | Valid |
| N07.8 | Hereditary nephropathy, not elsewhere classified with other morphologic lesions | Valid |
| N07.9 | Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions | Valid |
| N07.A | Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis | Valid |
| N07.B | Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD] | Valid |