- E72.09 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 E72.09 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E72.09 – other international versions of ICD-10 E72.09 may differ.
ICD-10-CM E72.09 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Fanconi (-de Toni) (-Debré) syndrome, unspecified
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 E72.09:
- diaper syndrome > Blue
- glycinuria > amino-acid E72.19
- renal transport NEC > amino-acid E72.19
- transport NEC > amino-acid E72.19
- nephrotic-glycosuric (with hypophosphatemic rickets) > Dwarfism E34.328
- hypophosphatemic with nephrotic-glycosuric dwarfism > Rickets (active) (acute) (adolescent) (chest wall) (congenital) (current) (infantile) (intestinal) E55.0
- with > renal N26.9
- cystine storage disease > with E72.09
- cystine > Stone (s)
- de Toni-Fanconi (-Debré) > Syndrome
- Fanconi (-de Toni) (-Debré) > Syndrome
- Lignac (de Toni) (-Fanconi) (-Debré) > Syndrome
- Toni-Fanconi > Syndrome