N07.9
BillableHereditary nephropathy, NEC w unsp morphologic lesions
Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- hypertensive chronic kidney disease (I12.-)
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- Alport's syndrome (Q87.81-)
- hereditary amyloid nephropathy (E85.-)
- nail patella syndrome (Q87.2)
- non-neuropathic heredofamilial amyloidosis (E85.-)
Code Also
A second code may be required; sequencing depends on circumstances
- any associated kidney failure (N17-N19).
Also Known As / Clinical Terms
SNOMED CT
- 10p partial monosomy syndrome6002006
- Bilateral paralysis6481005
- Diplegia6481005
- Parathyroid hyperplasia9092004
- Hereditary sensory neuropathy11442006
- Posterior sensory radicular neuropathy11442006
- Primary hyperparathyroidism36348003
- Choreoathetosis43105007
- Disorder of zinc metabolism46727001
- Spastic paralysis78403003
- Sensory neuropathy95662005
- Chronic deafness232325008
- Familial nephropathy236419006
- Progressive hereditary glomerulonephritis without deafness236419006
- Magnesium-losing nephropathy236479001
- Inherited magnesium-losing nephropathy236480003
- Marfanoid physique248298009
- Familial aplasia of the vermis253175003
- Idiopathic osteolyses254147009
- Carpal-tarsal osteolysis with nephropathy254149007
- Congenital nephritis276585000
- Spastic diplegia281411007
- Non-progressive hereditary glomerulonephritis399190000
- GN - Hereditary glomerulonephritis399340005
- Hereditary glomerulonephritis399340005
- Hereditary nephritis399340005
- Dent disease444645005
- Dent's disease444645005
- Autosomal dominant familial haematuria, retinal arteriolar tortuosity, contractures702428000
- Autosomal dominant familial hematuria, retinal arteriolar tortuosity, contractures702428000
- HANAC - hereditary angiopathy with nephropathy, aneurysms, and muscle cramps702428000
- HANAC syndrome702428000
- Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome702428000
- Autosomal dominant progressive nephropathy with hypertension703310005
- Joubert syndrome716997004
- Joubert syndrome with renal defect716999001
- Dent disease type 1717789008
- Dent disease type 2717790004
- Congenital cataract, nephropathy, encephalopathy syndrome722381004
- Crome syndrome722381004
- NSIAD - nephrogenic syndrome of inappropriate antidiuresis723440000
- Nephrogenic syndrome of inappropriate antidiuresis723440000
- Edwards Patton Dilly syndrome724093004
- Nephropathy, deafness, hyperparathyroidism syndrome724093004
- Barakat syndrome724282009
- HDR (hypoparathyroidism, sensorineural deafness, renal disease) syndrome724282009
- HDR syndrome724282009
- Hypoparathyroidism, deafness, renal disease syndrome724282009
- Deletion of part of chromosome 10726380001
- Deafness, small bowel diverticulosis, neuropathy syndrome733071009
- Groll Hirschowitz syndrome733071009
- Fitzsimmons Walson Mellor syndrome733089005
- Spastic paraplegia, nephritis, deafness syndrome733089005
- Microcephalus, glomerulonephritis, marfanoid habitus syndrome733472005
- Peripheral sensory neuropathy789588003
- Cerebrorenal syndrome Perez type1187043002
- Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome1187043002
- Hunter Jurenka Thompson syndrome1208341008
- ORC (oculo-renal-cerebellar) syndrome1208341008
- Oculorenocerebellar syndrome1208341008
- Severe oculo-renal-cerebellar syndrome1208341008
- Hereditary disorder of kidney367591000119105
- Hereditary nephropathy367591000119105
- Inherited renal disease367591000119105
- Progressive chorea27751000119104
Frequently Asked Questions
What is ICD-10 code N07.9?
ICD-10-CM code N07.9 represents "Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions". It is a billable/specific code that can be used on a claim.
Is N07.9 a billable code?
Yes, N07.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is N07.9 in?
N07.9 is in Chapter 14: Diseases of the Genitourinary System (codes N00-N99).
What codes cannot be used with N07.9?
N07.9 has Excludes1 notes indicating codes that cannot be used together with it, including: hypertensive chronic kidney disease (I12.-).
What SNOMED CT codes does N07.9 map to?
N07.9 maps to 41 SNOMED CT concepts: 6002006, 702428000, 703310005, 724282009, 6481005, and 36 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for N07.9?
N07.9 is linked to 1 UMLS Concept Unique Identifier: C2902925. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.