E85.9 AMYLOIDOSIS, UNSPECIFIED

Code Information

  • Diagnosis Code: E85.9
  • Short Description: Amyloidosis, unspecified
  • Long Description: Amyloidosis, unspecified
  • Code Version: 2025 ICD-10-CM

The code E85.9 is VALID for claim submission

Code Classification

Synonyms

  • Amyloid myopathy
  • Amyloidosis
  • Dilated cardiomyopathy due to amyloidosis
  • Dilated cardiomyopathy due to infiltration
  • Entrapment syndrome due to amyloid
  • Factor X deficiency
  • Factor X deficiency due to systemic amyloidosis
  • Glomerular disorder due to amyloidosis
  • Hypothyroidism due to amyloidosis
  • Hypothyroidism due to infiltrative disease
  • Infiltrative cardiomyopathy
  • Myocardial degeneration
  • Nephrotic syndrome associated with another disorder
  • Nephrotic syndrome in amyloidosis
  • Prothrombin complex deficiency
  • Restrictive cardiomyopathy secondary to amyloidosis
  • Secondary restrictive cardiomyopathy

Diagnostic Related Group(s)

The code E85.9 is grouped in the following Diagnostic Related Group(s) MS-DRG V42.0

  1. Connective Tissue Disorders With Mcc (545)
  2. Connective Tissue Disorders With Cc (546)
  3. Connective Tissue Disorders Without Cc/mcc (547)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E85.9 Right Arrow 277.30 Amyloidosis NOS
This ICD-10 to ICD-9 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-10 Code ICD-10 Description
E85 Amyloidosis
E85.0 Non-neuropathic heredofamilial amyloidosis
E85.1 Neuropathic heredofamilial amyloidosis
E85.2 Heredofamilial amyloidosis, unspecified
E85.3 Secondary systemic amyloidosis
E85.4 Organ-limited amyloidosis
E85.8 Other amyloidosis
E85.81 Light chain (AL) amyloidosis
E85.82 Wild-type transthyretin-related (ATTR) amyloidosis
E85.89 Other amyloidosis
This page was last updated on: 10/1/2024