Home > 2011 ICD-9-CM Diagnosis Codes > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Other Metabolic Disorders And Immunity Disorders 270-279 > Other and unspecified disorders of metabolism 277-
Specific code 2011 ICD-9-CM Diagnosis Code 277.39
Other amyloidosis
  • Short description: Amyloidosis NEC.
  • ICD-9-CM 277.39 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 277.39 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2011 version of ICD-9-CM 277.39.
  • More recent version(s) of ICD-9-CM 277.39: 2012 2013 2014 2015.
Convert to ICD-10-CM: 277.39 converts approximately to:
  • 2015/16 ICD-10-CM E85.1 Neuropathic heredofamilial amyloidosis
    Or:
  • 2015/16 ICD-10-CM E85.3 Secondary systemic amyloidosis
    Or:
  • 2015/16 ICD-10-CM E85.8 Other amyloidosis
Approximate Synonyms
  • 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
  • Cardiac amyloidosis
  • Cerebral amyloid angiopathy
  • 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 oculoleptomeningeal amyloid angiopathy
  • Heredofamilial systemic amyloidosis affecting skin
  • Hypothyroidism due to amyloidosis
  • Inherited systemic amyloidosis
  • Isolated atrial amyloid
  • Isolated corneal amyloidosis
  • Laryngeal amyloidosis
  • Localized amyloidosis
  • Localized hereditary amyloidosis
  • Localized non-hereditary amyloidosis
  • Macular amyloidosis
  • Macular cutaneous amyloidosis
  • Maculopapular amyloidosis
  • Meretoja syndrome
  • Myeloma-associated primary systemic amyloidosis
  • Nephrotic syndrome in amyloidosis
  • Neuropathic heredofamilial 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 amyloidosis
  • Primary systemic amyloidosis associated with occult plasma cell dyscrasia
  • Primary systemic amyloidosis with pseudoscleroderma
  • Pulmonary amyloidosis
  • Reactive systemic amyloidosis
  • Renal AA amyloidosis
  • Renal AL amyloidosis
  • Renal amyloid
  • Renal amyloidosis
  • Sago spleen
  • Secondary amyloidosis
  • 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
Applies To
  • Hereditary cardiac amyloidosis
  • Inherited systemic amyloidosis
  • Neuropathic (Portuguese) (Swiss) amyloidosis
  • Secondary amyloidosis
ICD-9-CM Volume 2 Index entries containing back-references to 277.39:
  • Abercrombie's syndrome (amyloid degeneration) 277.39
  • Amyloidosis (familial) (general) (generalized) (genetic) (primary) 277.30
    • cardiac, hereditary 277.39
    • secondary 277.39
    • systemic, inherited 277.39
  • Degeneration, degenerative
    • amyloid (any site) (general) 277.39
    • artery, arterial (atheromatous) (calcareous) - see also Arteriosclerosis
      • amyloid 277.39
      • lardaceous 277.39
      • medial NEC (see also Arteriosclerosis, extremities) 440.20
    • bacony (any site) 277.39
    • capillaries 448.9
      • amyloid 277.39
      • fatty 448.9
      • lardaceous 277.39
    • chitinous 277.39
    • cutis 709.3
      • amyloid 277.39
    • intestine 569.89
      • amyloid 277.39
      • lardaceous 277.39
    • lardaceous (any site) 277.39
    • liver (diffuse) 572.8
      • amyloid 277.39
      • congenital (cystic) 751.62
      • cystic 572.8
      • fatty 571.8
      • hypertrophic 572.8
      • lardaceous 277.39
      • parenchymatous, acute or subacute (see also Necrosis, liver) 570
      • pigmentary 572.8
      • toxic (acute) 573.8
      • waxy 277.39
    • spinal (cord) 336.8
      • amyloid 277.39
      • column 733.90
      • combined (subacute) (see also Degeneration, combined) 266.2 [336.2]
      • dorsolateral (see also Degeneration, combined) 266.2 [336.2]
      • familial NEC 336.8
      • fatty 336.8
      • funicular (see also Degeneration, combined) 266.2 [336.2]
      • heredofamilial NEC 336.8
      • posterolateral (see also Degeneration, combined) 266.2 [336.2]
      • subacute combined - see Degeneration, combined
      • tuberculous (see also Tuberculosis) 013.8
    • spleen 289.59
      • amyloid 277.39
      • lardaceous 277.39
    • stomach 537.89
      • lardaceous 277.39
    • waxy (any site) 277.39
  • Disease, diseased - see also Syndrome
    • gastrointestinal (tract) 569.9
    • lardaceous (any site) 277.39
    • spleen (organic) (postinfectional) 289.50
      • amyloid 277.39
      • lardaceous 277.39
      • polycystic 759.0
      • specified NEC 289.59
    • stomach NEC (organic) 537.9
      • functional 536.9
      • lardaceous 277.39
    • thyroid (gland) NEC 246.9
      • heart (see also Hyperthyroidism) 242.9 [425.7]
      • lardaceous 277.39
      • specified NEC 246.8
    • waxy (any site) 277.39
  • Gammaloidosis 277.39
  • Infiltrate, infiltration
    • amyloid (any site) (generalized) 277.39
  • Lardaceous
    • degeneration (any site) 277.39
    • disease 277.39
    • liver 277.39
  • Large
    • waxy liver 277.39
  • Sago spleen 277.39
  • Syndrome - see also Disease
    • Abercrombie's (amyloid degeneration) 277.39
  • Thesaurismosis
    • amyloid 277.39
  • Waxy
    • degeneration, any site 277.39
    • disease 277.39
    • liver (large) 277.39
    • spleen 277.39
 277.31 ICD9Data.com 277.4 
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 277.39 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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