Familial aplasia of the vermis
Fitzsimmons Walson Mellor syndrome
Disorder of zinc metabolism
Congenital cataract, nephropathy, encephalopathy syndrome
Deafness, small bowel diverticulosis, neuropathy syndrome
Dent disease
Hereditary nephritis
Non-progressive hereditary glomerulonephritis
Magnesium-losing nephropathy
Joubert syndrome
Severe oculo-renal-cerebellar syndrome
HANAC - hereditary angiopathy with nephropathy, aneurysms, and muscle cramps
Deletion of part of chromosome 10
Dent disease type 2
Autosomal dominant familial haematuria, retinal arteriolar tortuosity, contractures
Hereditary sensory neuropathy
Hereditary disorder of kidney
Idiopathic osteolyses
Inherited magnesium-losing nephropathy
Marfanoid physique
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome
Diplegia
Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
Autosomal dominant progressive nephropathy with hypertension
HDR syndrome
Posterior sensory radicular neuropathy
Barakat syndrome
Edwards Patton Dilly syndrome
Groll Hirschowitz syndrome
Peripheral sensory neuropathy
Choreoathetosis
Parathyroid hyperplasia
HDR (hypoparathyroidism, sensorineural deafness, renal disease) syndrome
Joubert syndrome with renal defect
Hunter Jurenka Thompson syndrome
Familial nephropathy
Spastic diplegia
Dent's disease
Hypoparathyroidism, deafness, renal disease syndrome
Progressive chorea
GN - Hereditary glomerulonephritis
Hereditary glomerulonephritis
Chronic deafness
Dent disease type 1
Nephropathy, deafness, hyperparathyroidism syndrome
Sensory neuropathy
HANAC syndrome
Primary hyperparathyroidism
Oculorenocerebellar syndrome
Crome syndrome
Cerebrorenal syndrome Perez type
Inherited renal disease
Bilateral paralysis
Autosomal dominant familial hematuria, retinal arteriolar tortuosity, contractures
Hereditary nephropathy
NSIAD - nephrogenic syndrome of inappropriate antidiuresis
Microcephalus, glomerulonephritis, marfanoid habitus syndrome
Spastic paraplegia, nephritis, deafness syndrome
Spastic paralysis
Congenital nephritis
Nephrogenic syndrome of inappropriate antidiuresis
Progressive hereditary glomerulonephritis without deafness
10p partial monosomy syndrome
ORC (oculo-renal-cerebellar) syndrome
Carpal-tarsal osteolysis with nephropathy

Frequently Asked Questions

What is the ICD-10 code for hereditary nephropathy, nec w unsp morphologic lesions?

The ICD-10-CM code for hereditary nephropathy, nec w unsp morphologic lesions is N07.9. The full clinical description is "Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions". N07.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code N07.9 mean?

ICD-10-CM code N07.9 represents “Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions”. 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 N07.9 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.

How does N07.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary nephropathy, nec w unsp morphologic lesions 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 N07.9?

N07.9 maps to the ICD-11 code: MF8Z (Clinical findings in specimens from the urinary system, 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.