ICD-9 Diagnosis Code 277.39

Amyloidosis NEC

Diagnosis Code 277.39

ICD-9: 277.39
Short Description: Amyloidosis NEC
Long Description: Other amyloidosis
This is the 2014 version of the ICD-9-CM diagnosis code 277.39

Code Classification
  • Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279)
    • Other metabolic disorders and immunity disorders (270-279)
      • 277 Other and unspecified disorders of metabolism

Information for Medical Professionals

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The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • AA amyloid nephropathy
  • AA amyloidosis
  • AD type amyloidosis
  • Age-related amyloidosis
  • AL amyloid nephropathy
  • AL amyloidosis
  • Amyloid corneal degeneration
  • Amyloid disease of the urethra
  • Amyloid myopathy
  • Amyloid nephropathy
  • Amyloid of bladder
  • Amyloid of cornea
  • Amyloid of prostate
  • Amyloid of testes
  • Amyloid of ureter
  • Amyloid of vitreous
  • Amyloidogenic transthyretin amyloidosis
  • Amyloidosis limited to skin
  • Amyloidosis of skin
  • Amyloidosis of spleen
  • Autonomic neuropathy due to amyloid
  • Beta-2 microglobulin arthropathy
  • Bullous cutaneous amyloidosis
  • Cerebral amyloid angiopathy
  • Cerebral amyloid angiopathy associated with systemic amyloidosis
  • Cerebrovascular amyloidosis
  • Conjunctival amyloidosis
  • Cutaneous amyloidosis
  • Danish type familial amyloid cardiomyopathy
  • Dilated cardiomyopathy secondary to amyloidosis
  • Dominant primary localized cutaneous amyloidosis
  • Familial amyloid nephropathy with urticaria AND deafness
  • Familial amyloid neuropathy, Finnish type
  • Familial amyloid polyneuropathy
  • Familial amyloid polyneuropathy with cutaneous amyloidosis
  • Familial amyloid polyneuropathy, Iowa type
  • Familial amyloid polyneuropathy, type II
  • Familial amyloid polyneuropathy, type VI
  • Familial lichen amyloidosis
  • Familial localized cutaneous amyloidosis
  • Familial non-neuropathic amyloidosis
  • Familial visceral amyloidosis, Ostertag type
  • Gingival amyloidosis
  • Hemodialysis-associated secondary amyloidosis of skin
  • Hepatic amyloidosis
  • Hereditary cerebral amyloid angiopathy, Dutch type
  • Hereditary cerebral amyloid angiopathy, Icelandic type
  • Hereditary cerebrovascular amyloidosis
  • Hereditary cystatin C amyloid angiopathy
  • Hereditary oculoleptomeningeal amyloid angiopathy
  • Heredofamilial systemic amyloidosis affecting skin
  • Hypothyroidism due to amyloidosis
  • Isolated atrial amyloid
  • Isolated corneal amyloidosis
  • Laryngeal amyloidosis
  • Localized amyloidosis
  • Localized hereditary amyloidosis
  • Localized non-hereditary amyloidosis
  • Macular cutaneous amyloidosis
  • Maculopapular amyloidosis
  • Meretoja syndrome
  • Myeloma-associated primary systemic amyloidosis
  • Nephrotic syndrome in amyloidosis
  • Neuropathy in secondary amyloidosis
  • Nodular amyloidosis
  • Ocular amyloid deposit
  • Papular cutaneous amyloid
  • Poikilodermal cutaneous amyloid
  • Polyneuropathy in amyloidosis
  • Primary amyloidosis of light chain type
  • Primary familial amyloid myopathy
  • Primary sporadic amyloid myopathy
  • Primary systemic
  • Primary systemic amyloidosis associated with occult plasma cell dyscrasia
  • Primary systemic amyloidosis with pseudoscleroderma
  • Pulmonary amyloidosis
  • Reactive systemic amyloidosis
  • Sago spleen
  • Secondary localized cutaneous amyloidosis
  • Secondary systemic amyloidosis affecting skin
  • Senile brain amyloidosis
  • Senile cardiac amyloidosis
  • Senile systemic amyloidosis
  • Sporadic primary amyloidosis
  • Systemic amyloidosis
  • Systemic amyloidosis affecting skin

Index of Diseases and Injuries
References found for the code 277.39 in the Index of Diseases and Injuries:

Information for Patients


Amyloidosis occurs when abnormal proteins called amyloids build up and form deposits. The deposits can collect in organs such as the kidney and heart. This can cause the organs to become stiff and unable to work the way they should.

There are three main types of amyloidosis:

  • Primary - with no known cause
  • Secondary - caused by another disease, including some types of cancer
  • Familial - passed down through genes

Symptoms can vary, depending upon which organs are affected. Treatment depends on the type of amyloidosis you have. The goal is to help with symptoms and limit the production of proteins. If another disease is the cause, it needs to be treated.

  • Abdominal wall fat pad biopsy
  • Cardiac amyloidosis
  • Carpal tunnel biopsy
  • Hereditary amyloidosis
  • Primary amyloidosis
  • Secondary systemic amyloidosis

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