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277.39 - Other Amyloidosis

The ICD 9 Code for Other amyloidosis is listed as 277.39.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
ICD 9 CM Field Value
Diagnosis Code: 277.39
Long Description: Other amyloidosis
Short Description: Amyloidosis NEC
Chapter: Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders
Block: Other Metabolic Disorders And Immunity Disorders (270-279)
Related Descriptions: 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
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
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 (AL fibril type) amyloidosis
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 (AA fibril type)
Senile brain amyloidosis
Senile cardiac amyloidosis
Senile systemic amyloidosis
Sporadic primary amyloidosis
Systemic amyloidosis
Systemic amyloidosis affecting skin
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD-10-CM Code: E85.1 - Neuropathic heredofamilial amyloidosis (approximate)
ICD-10-CM Code: E85.3 - Secondary systemic amyloidosis (approximate)
ICD-10-CM Code: E85.8 - Other amyloidosis (approximate)
ICD-9-CM Siblings (same level / similar specificity) of 277.39:
277.30 - Amyloidosis, unspecified
277.31 - Familial Mediterranean fever