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 | |