E72.09
Other disorders of amino-acid transport
Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 14 never code together
E72code
E70-E88block
E00-E89chapter
Excludes1
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)P70-P74
Excludes1 — never code together. The excluded condition and this one are mutually exclusive.
Excludes2 — not included here, but the patient may have both. Code both when documented.
Instructional notes 2
E72.09code
Inclusion terms
- Fanconi (-de Toni) (-Debré) syndrome, unspecified
E00-E89chapter
Notes
- All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.E05.8E07.0E16-E31E34.-
Index entries leading here 13
- Disorder (of) — see also Disease
- Beta-mercaptolactate-cysteine disulfiduria E72.09
- Blue
- diaper syndrome E72.09
- Stone (s) — see also Calculus
- cystine E72.09
- Sclerosis, sclerotic
- Syndrome — see also Disease
- De Toni-Fanconi (-Debré) syndrome E72.09
- Dwarfism E34.328
- nephrotic-glycosuric (with hypophosphatemic rickets) E72.09
- Fanconi (-de Toni)(-Debré) syndrome E72.09
- Glycinuria (renal) (with ketosis) E72.09
- Rickets (active) (acute) (adolescent) (chest wall) (congenital) (current) (infantile) (intestinal) E55.0
- hypophosphatemic with nephrotic-glycosuric dwarfism E72.09
- Lignac (-de Toni) (-Fanconi) (-Debré) disease or syndrome E72.09
- Toni-Fanconi syndrome (cystinosis) E72.09
Alongside this code 5 same parent — E72.0
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.