N07.5
Billable codeHereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
The ICD-10 code for hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis is N07.5.
Clinical notes
Excludes1 (not coded here)
An Excludes1 note is a pure exclusion: the excluded condition and this code should never be reported together, because the two conditions cannot occur at the same time (e.g. a congenital form vs. an acquired form of the same disease).
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, types 1 and 3, or NOS
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •Confirm the excluded condition(s) listed above are not also present — Excludes1 conditions cannot be coded together with this one.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- 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
- N07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
- N07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative 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]
- N07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
ICD-9-CM equivalent
Informational only — GEM mappings are approximate, not guaranteed one-to-one equivalents. Verify before use in billing.
- 5832Approximate match
Associated MS-DRGs
N07.5 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.