N07.5
BillableHereditary nephropathy, NEC w diffuse mesangiocap glomrlneph
Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, types 1 and 3, or NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •Alport's syndromeQ87.81
- •hereditary amyloid nephropathyE85
- •nail patella syndromeQ87.2
- •non-neuropathic heredofamilial amyloidosisE85
Code Also
A second code may be required; sequencing depends on circumstances
Related Codes(10)
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
N07.6Hereditary 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
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(12)
SNOMED CT
UMLS
Clinical Terms
- Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, types 1 and 3, or NOS
- Mesangiocapillary glomerulonephritis type III
- Hereditary diffuse mesangiocapillary glomerulonephritis
- MCGN (mesangiocapillary glomerulonephritis) type III
- Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III
Frequently Asked Questions
What is the ICD-10 code for hereditary nephropathy, nec w diffuse mesangiocap glomrlneph?
The ICD-10-CM code for hereditary nephropathy, nec w diffuse mesangiocap glomrlneph is N07.5. The full clinical description is "Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis". N07.5 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code N07.5 mean?
ICD-10-CM code N07.5 represents “Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis”. It is classified under Chapter 14: Diseases of the Genitourinary System and is a billable/specific code that can be used on a claim.
Is N07.5 a billable code?
Yes, N07.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is N07.5 in?
N07.5 is in Chapter 14: Diseases of the Genitourinary System (codes N00-N99).
What codes cannot be used with N07.5?
N07.5 has Excludes1 notes indicating codes that cannot be used together with it, including: hypertensive chronic kidney disease (I12.-); Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis (N07.A); Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy (N07.A).
What SNOMED CT codes does N07.5 map to?
N07.5 maps to 3 SNOMED CT concepts: 367561000119103, 368941000119108, 236409000. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for N07.5?
N07.5 is linked to 2 UMLS Concept Unique Identifiers: C0868881, C2902920. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does N07.5 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary nephropathy, nec w diffuse mesangiocap glomrlneph affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of N07.5?
N07.5 maps to the ICD-11 code: GB4Z (Glomerular diseases, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.