- E85.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM E85.0 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E85.0 – other international versions of ICD-10 E85.0 may differ.
ICD-10-CM E85.0 is grouped within Diagnostic Related Group(s):
- 545 Connective tissue disorders with mcc
- 546 Connective tissue disorders with cc
- 547 Connective tissue disorders without cc/mcc
Applicable To
- Hereditary amyloid nephropathy
Type 2 Excludes
- Transthyretin-related (ATTR) familial amyloid cardiomyopathy (E85.4)
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to E85.0:
- non-neuropathic heredofamilial > Amyloidosis (generalized) (primary) E85.9
- amyloidosis > in (due to) E27.1
- amyloid, hereditary > Nephropathy N28.9
- paroxysmal, familial > Peritonitis (adhesive) (bacterial) (fibrinous) (hemorrhagic) (idiopathic) (localized) (perforative) (primary) (with adhesions) (with effusion) K65.9
- benign > paroxysmal, familial E85.0
- periodic, familial > Peritonitis (adhesive) (bacterial) (fibrinous) (hemorrhagic) (idiopathic) (localized) (perforative) (primary) (with adhesions) (with effusion) K65.9
- periodic, familial > Polyserositis