E72.04
BillableCystinosis
Cystinosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Fanconi (-de Toni) (-Debré) syndrome with cystinosis
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout (M1A.-, M10.-)
- disorders of tryptophan metabolism (E70.5)
- Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Adolescent cystinosis22830006
- Cystinosis, type II22830006
- Intermediate cystinosis22830006
- Juvenile cystinosis22830006
- Juvenile nephropathic cystinosis22830006
- Late-onset cystinosis22830006
- Benign adult cystinosis25010000
- Benign adult nephropathic cystinosis25010000
- Benign cystinosis25010000
- Hypothyroidism due to infiltrative disease30229009
- Hypothyroidism due to cystinosis42785009
- Infantile nephropathic cystinosis62332007
- Lignac-Fanconi syndrome62332007
- Nephropathic cystinosis62332007
- Cystine diathesis190681003
- Cystine disease190681003
- Cystine storage disease190681003
- Cystinosis190681003
- Congenital Fanconi syndrome236466005
- De Toni-Fanconi syndrome236466005
- Primary Fanconi syndrome236466005
- Renal tubulo-interstitial disorder due to cystinosis1187546002
- Tubulointerstitial nephritis due to cystinosis1187546002
UMLS
- CYSTINOSIN, DEFECT OFC4316899
- Cystine DiathesesC4316899
- Cystine DiathesisC4316899
- Cystine DiseaseC4316899
- Cystine DiseasesC4316899
- Cystine Storage DiseaseC4316899
- Cystine Storage DiseasesC4316899
- Cystine diathesisC4316899
- Cystine diseaseC4316899
- Cystine storage diseaseC4316899
- CystinosesC4316899
- Cystinosin, Defect ofC4316899
- CystinosisC4316899
- Cystinosis (disorder)C4316899
- Defect of CystinosinC4316899
- Diatheses, CystineC4316899
- Diathesis, CystineC4316899
- LYSOSOMAL CYSTINE TRANSPORT PROTEIN, DEFECT OFC4316899
- Lysosomal Cystine Transport Protein, Defect OfC4316899
- Storage Disease, CystineC4316899
- Storage Diseases, CystineC4316899
- cystine storage diseaseC4316899
- cystinosisC4316899
- Fanconi (-de Toni) (-Debré) syndrome with cystinosisC2874257
Frequently Asked Questions
What is ICD-10 code E72.04?
ICD-10-CM code E72.04 represents "Cystinosis". It is a billable/specific code that can be used on a claim.
Is E72.04 a billable code?
Yes, E72.04 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.04 in?
E72.04 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.04?
E72.04 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 11 more.
What SNOMED CT codes does E72.04 map to?
E72.04 maps to 8 SNOMED CT concepts: 22830006, 25010000, 236466005, 190681003, 42785009, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.04?
E72.04 is linked to 2 UMLS Concept Unique Identifiers: C4316899, C2874257. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.