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Diagnosis Code

N07.9 HEREDITARY NEPHROPATHY, NEC W UNSP MORPHOLOGIC LESIONS


Code Information

Diagnosis Code: N07.9

Short Description: Hereditary nephropathy, NEC w unsp morphologic lesions

Long Description: Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions

The code N07.9 is VALID for claim submission

Code Classification:

  • Diseases of the genitourinary system (N00–N99)
    • Glomerular diseases (N00-N08)
      • Hereditary nephropathy, not elsewhere classified (N07)
        • N07.9 Hereditary nephropathy, NEC w unsp morphologic lesions

Code Version: 2022 ICD-10-CM


Synonyms

  • 10p partial monosomy syndrome
  • Autosomal dominant complex hereditary spastic paraplegia
  • Autosomal dominant progressive nephropathy with hypertension
  • Carpal-tarsal osteolysis with nephropathy
  • Choreoathetosis
  • Chronic deafness
  • Congenital nephritis
  • Crome syndrome
  • Deafness, small bowel diverticulosis, neuropathy syndrome
  • Deletion of part of chromosome 10
  • Dent disease type 1
  • Dent disease type 2
  • Dent's disease
  • Diplegia
  • Disorder of zinc metabolism
  • Familial aplasia of the vermis
  • Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
  • Hereditary nephritis
  • Hereditary nephropathy
  • Hereditary sensory neuropathy
  • Hypoparathyroidism, deafness, renal disease syndrome
  • Idiopathic osteolyses
  • Inherited magnesium-losing nephropathy
  • Joubert syndrome
  • Joubert syndrome with renal defect
  • Magnesium-losing nephropathy
  • Marfanoid physique
  • Microcephalus, glomerulonephritis, marfanoid habitus syndrome
  • Nephrogenic syndrome of inappropriate antidiuresis
  • Nephropathy, deafness, hyperparathyroidism syndrome
  • Non-progressive hereditary glomerulonephritis
  • Parathyroid hyperplasia
  • Peripheral sensory neuropathy
  • Primary hyperparathyroidism
  • Progressive hereditary glomerulonephritis without deafness
  • Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome
  • Sensory neuropathy
  • Severe oculo-renal-cerebellar syndrome
  • Spastic diplegia
  • Spastic paralysis
  • Spastic paraplegia, nephritis, deafness syndrome

Diagnostic Related Group(s)

The code N07.9 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Kidney And Urinary Tract Diagnoses With Mcc (698)
  • Other Kidney And Urinary Tract Diagnoses With Cc (699)
  • Other Kidney And Urinary Tract Diagnoses Without Cc/mcc (700)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
N07.9 Right Arrow 583.9 Nephritis NOS

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
N07 Hereditary nephropathy, not elsewhere classified
N07.0 Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
N07.1 Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
N07.2 Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
N07.3 Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
N07.4 Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
N07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
N07.6 Hereditary nephropathy, not elsewhere classified with dense deposit disease
N07.7 Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
N07.8 Hereditary nephropathy, not elsewhere classified with other morphologic lesions
N07.A Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis

This page was last updated on: 10/1/2023

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