- E72.04 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 E72.04 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E72.04 – other international versions of ICD-10 E72.04 may differ.
ICD-10-CM E72.04 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Fanconi (-de Toni) (-Debré) syndrome with cystinosis
Type 1 Excludes
- Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09)
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 E72.04:
- with cystinosis > De Toni-Fanconi syndrome (-Debré) E72.09
- Lignac\’s (cystinosis) > Disease, diseased
- cystinosis > amino-acid E72.19
- cystinosis > tubulo-interstitial (in) A23.9
- with cystinosis > Fanconi syndrome (-de Toni)(-Debré) E72.09
- with cystinosis > Lignac disease or syndrome (-de Toni) (-Fanconi) (-Debré) E72.09
- cystinosis > in (due to) A23.9
- with cystinosis > de Toni-Fanconi (-Debré) E72.09
- with cystinosis > Fanconi (-de Toni) (-Debré) E72.09
- with cystinosis > Lignac (de Toni) (-Fanconi) (-Debré) E72.09
- with cystinosis > Toni-Fanconi E72.09
- with cystinosis > Toni-Fanconi syndrome (cystinosis) E72.09