N07.B
ICD-10BillableHereditary nephrop, NEC with APOL1-mediated kidney disease
Official ICD-10-CM descriptor (FY2026)
Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]
N07.B is valid for submission on a claim — CMS flags it as a billable, specific code.
Inclusion terms
- AMKD (with glomerulonephritis)
- AMKD (with glomerulosclerosis)
Related codes in N07
- N07.0Hereditary nephropathy, NEC w minor glomerular abnormality
- N07.1Heredit nephrop, NEC w focal and seg glomerular lesions
- N07.2Hereditary nephropathy, NEC w diffuse membranous glomrlneph
- N07.3Heredit nephrop, NEC w diffuse mesangial prolif glomrlneph
- N07.4Heredit nephrop, NEC w diffus endocaplry prolif glomrlneph
- N07.5Hereditary nephropathy, NEC w diffuse mesangiocap glomrlneph
- N07.6Hereditary nephropathy, NEC w dense deposit disease
- N07.7Hereditary nephropathy, NEC w diffuse crescentic glomrlneph
- N07.8Hereditary nephropathy, NEC w oth morphologic lesions
- N07.9Hereditary nephropathy, NEC w unsp morphologic lesions
- N07.AHereditary nephropathy, NEC with C3 glomerulonephritis
Where this code sits
- Parent code
- N07
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ICD-10-CM FY2026. Centers for Medicare & Medicaid Services (CMS) / National Center for Health Statistics (NCHS), “2026 ICD-10-CM Code Descriptions in Tabular Order” (icd10cm_order_2026.txt). Download the original file from cms.gov. Public domain (US Government work). Descriptors, billable flags and instructional notes on this page are reproduced from that file without modification. Krasyn adds no clinical guidance.