277.39 AMYLOIDOSIS NEC


Code Information

Diagnosis Code: 277.39

Short Description: Amyloidosis NEC

Long Description: Other amyloidosis

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
        • 277.39 Amyloidosis NEC

Code Version: 2015 ICD-9-CM


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
  • 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

References to Index of Diseases and Injuries

The code 277.39 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Abercrombie's syndrome (amyloid degeneration) 277.39
  • Amyloid disease or degeneration 277.30
    • heart 277.39 [425.7]
  • Amyloidosis (familial) (general) (generalized) (genetic) (primary) 277.30
    • with lung involvement 277.39 [517.8]
    • cardiac, hereditary 277.39
    • heart 277.39 [425.7]
    • nephropathic 277.39 [583.81]
    • neuropathic (Portuguese) (Swiss) 277.39 [357.4]
    • pulmonary 277.39 [517.8]
    • secondary 277.39
    • systemic, inherited 277.39
  • Arthritis, arthritic (acute) (chronic) (subacute) 716.9
    • due to or associated with
      • amyloidosis 277.39 [713.7]
  • Cardiomyopathy (congestive) (constrictive) (familial) (infiltrative) (obstructive) (restrictive) (sporadic) 425.4
    • amyloid 277.39 [425.7]
    • due to
      • amyloidosis 277.39 [425.7]
    • metabolic NEC 277.9 [425.7]
      • amyloid 277.39 [425.7]
  • Degeneration, degenerative
    • adrenal (capsule) (gland) 255.8
      • lardaceous 277.39
    • amyloid (any site) (general) 277.39
    • artery, arterial (atheromatous) (calcareous) - see also Arteriosclerosis
      • amyloid 277.39
      • lardaceous 277.39
    • bacony (any site) 277.39
    • capillaries 448.9
      • amyloid 277.39
      • lardaceous 277.39
    • chitinous 277.39
    • conjunctiva 372.50
      • amyloid 277.39 [372.50]
    • cutis 709.3
      • amyloid 277.39
    • heart (brown) (calcareous) (fatty) (fibrous) (hyaline) (mural) (muscular) (pigmentary) (senile) (with arteriosclerosis) (see also Degeneration, myocardial) 429.1
      • amyloid 277.39 [425.7]
    • intestine 569.89
      • amyloid 277.39
      • lardaceous 277.39
    • kidney (see also Sclerosis, renal) 587
      • amyloid 277.39 [583.81]
      • lardaceous 277.39 [583.81]
      • waxy 277.39 [583.81]
    • lardaceous (any site) 277.39
    • liver (diffuse) 572.8
      • amyloid 277.39
      • lardaceous 277.39
      • waxy 277.39
    • lymph gland 289.3
      • lardaceous 277.39
    • myocardium, myocardial (brown) (calcareous) (fatty) (fibrous) (hyaline) (mural) (muscular) (pigmentary) (senile) (with arteriosclerosis) 429.1
      • amyloid 277.39[425.7]
    • nervous system 349.89
      • amyloid 277.39 [357.4]
    • skin 709.3
      • amyloid 277.39
    • spinal (cord) 336.8
      • amyloid 277.39
    • spleen 289.59
      • amyloid 277.39
      • lardaceous 277.39
    • stomach 537.89
      • lardaceous 277.39
    • thymus (gland) 254.8
      • lardaceous 277.39
    • waxy (any site) 277.39
  • Disease, diseased - see also Syndrome
    • gastrointestinal (tract) 569.9
      • amyloid 277.39
    • heart (organic) 429.9
      • amyloid 277.39[425.7]
      • due to
        • amyloidosis 277.39[425.7]
    • intestine 569.9
      • lardaceous 277.39
    • lardaceous (any site) 277.39
    • lung NEC 518.89
      • in
        • amyloidosis 277.39 [517.8]
    • pulmonary - see also Disease, lung
      • amyloid 277.39 [517.8]
    • renal (functional) (pelvis) (see also Disease, kidney) 593.9
      • due to
        • amyloidosis 277.39 [583.81]
    • spleen (organic) (postinfectional) 289.50
      • amyloid 277.39
      • lardaceous 277.39
    • stomach NEC (organic) 537.9
      • lardaceous 277.39
    • thyroid (gland) NEC 246.9
      • lardaceous 277.39
    • waxy (any site) 277.39
  • Gammaloidosis 277.39
  • Glomerulonephritis (see also Nephritis) 583.9
    • due to or associated with
      • amyloidosis 277.39 [583.81]
        • with nephrotic syndrome 277.39 [581.81]
        • chronic 277.39 [582.81]
  • Infiltrate, infiltration
    • amyloid (any site) (generalized) 277.39
  • Lardaceous
    • degeneration (any site) 277.39
    • disease 277.39
    • kidney 277.39 [583.81]
    • liver 277.39
  • Large
    • waxy liver 277.39
  • Laryngitis (acute) (edematous) (fibrinous) (gangrenous) (infective) (infiltrative) (malignant) (membranous) (phlegmonous) (pneumococcal) (pseudomembranous) (septic) (subglottic) (suppurative) (ulcerative) (viral) 464.00
  • Myocardiopathy (congestive) (constrictive) (familial) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic) 425.4
    • amyloid 277.39 [425.7]
    • due to
      • amyloidosis 277.39 [425.7]
  • Myopathy 359.9
    • amyloid 277.39 [359.6]
    • in
      • amyloidosis 277.39 [359.6]
  • Nephritis, nephritic (albuminuric) (azotemic) (congenital) (degenerative) (diffuse) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) 583.9
    • amyloid 277.39 [583.81]
      • chronic 277.39 [582.81]
    • due to
      • amyloidosis 277.39 [583.81]
        • chronic 277.39 [582.81]
  • Nephrosis, nephrotic (Epstein's) (syndrome) 581.9
    • in
      • amyloidosis 277.39 [581.81]
  • Neuritis (see also Neuralgia) 729.2
    • amyloid, any site 277.39 [357.4]
  • Neuropathy, neuropathic (see also Disorder, nerve) 355.9
    • peripheral (nerve) (see also Polyneuropathy) 356.9
      • autonomic 337.9
        • amyloid 277.39 [337.1]
        • in
          • amyloidosis 277.39 [337.1]
  • Polyneuropathy (peripheral) 356.9
    • amyloid 277.39 [357.4]
    • in
      • amyloidosis 277.39 [357.4]
  • 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
    • kidney 277.39 [583.81]
    • liver (large) 277.39
    • spleen 277.39

Crosswalk Information

The code 277.39 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
277.39 Right Arrow E85.1 Neuropathic heredofamilial amyloidosis
E85.3 Secondary systemic amyloidosis
E85.8 Other amyloidosis
This ICD-9 to ICD-10 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-9 Code ICD-9 Description
277.00 Cystic fibrosis without mention of meconium ileus
277.01 Cystic fibrosis with meconium ileus
277.02 Cystic fibrosis with pulmonary manifestations
277.03 Cystic fibrosis with gastrointestinal manifestations
277.09 Cystic fibrosis with other manifestations
277.1 Disorders of porphyrin metabolism
277.2 Other disorders of purine and pyrimidine metabolism
277.30 Amyloidosis, unspecified
277.31 Familial Mediterranean fever
277.4 Disorders of bilirubin excretion
277.5 Mucopolysaccharidosis
277.6 Other deficiencies of circulating enzymes
277.7 Dysmetabolic syndrome X
277.81 Primary carnitine deficiency
277.82 Carnitine deficiency due to inborn errors of metabolism
277.83 Iatrogenic carnitine deficiency
277.84 Other secondary carnitine deficiency
277.85 Disorders of fatty acid oxidation
277.86 Peroxisomal disorders
277.87 Disorders of mitochondrial metabolism
277.88 Tumor lysis syndrome
277.89 Other specified disorders of metabolism
277.9 Unspecified disorder of metabolism


This page was last updated on: 10/1/2014