Abderhalden-Kaufmann-Lignac syndrome (cystinosis) E72.04
(AKL syndrome), also called nephropathic cystinosis, is an autosomal recessive renal disorder of childhood comprising cystinosis and renal rickets.
E72.04 is a billable ICD code used to specify a diagnosis of cystinosis. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
(AKL syndrome), also called nephropathic cystinosis, is an autosomal recessive renal disorder of childhood comprising cystinosis and renal rickets.
E72.04 is a billable ICD code used to specify a diagnosis of cystinosis. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
Coding Notes for E72.04 Info for medical coders on how to properly use this ICD-10 code
- Inclusion Terms:
- Fanconi (-de Toni) (-Debré) syndrome with cystinosis
- Code Type-1 Excludes:
- Fanconi (-de Toni) (-Debré) syndrome without cystinosis - instead, use code E72.09
MS-DRG Mapping
- DRG Group #642 - Inborn and other disorders of metabolism.
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