2012 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 2012 version of ICD-9-CM 277.39.
- More recent version(s) of ICD-9-CM 277.39: 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
- adrenal (capsule) (gland) 255.8
- 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
- amyloid 277.39
- functional 536.9
- 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