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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- disorders of:
- •aromatic amino-acid metabolismE70
- •branched-chain amino-acid metabolismE71.0-E71.2
- •fatty-acid metabolismE71.3
- •purine and pyrimidine metabolismE79
- •gout (M1A.-,M10
- •disorders of tryptophan metabolismE70.5
- •Fanconi (-de Toni) (-Debré) syndrome without cystinosisE72.09
Related Codes(5)
Also Known As / Clinical Terms(82)
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
Clinical Terms
- CYSTINOSIN, DEFECT OF
- Late-onset cystinosis
- Cystine storage disease
- Cystine Diseases
- Benign cystinosis
- Nephropathic cystinosis
- Defect of Cystinosin
- Cystine Disease
- LYSOSOMAL CYSTINE TRANSPORT PROTEIN, DEFECT OF
- De Toni-Fanconi syndrome
- Intermediate cystinosis
- Renal tubulo-interstitial disorder due to cystinosis
- Benign adult nephropathic cystinosis
- Lignac-Fanconi syndrome
- Hypothyroidism due to infiltrative disease
- Adolescent cystinosis
- Juvenile nephropathic cystinosis
- Hypothyroidism due to cystinosis
- Cystine diathesis
- Storage Disease, Cystine
- Cystinosis, type II
- Diatheses, Cystine
- Fanconi (-de Toni) (-Debré) syndrome with cystinosis
- Benign adult cystinosis
- Storage Diseases, Cystine
- Cystine Storage Diseases
- Juvenile cystinosis
- Congenital Fanconi syndrome
- Primary Fanconi syndrome
- Infantile nephropathic cystinosis
- Tubulointerstitial nephritis due to cystinosis
- Cystine Diatheses
- Cystinoses
- Diathesis, Cystine
- Cystinosis (disorder)
Frequently Asked Questions
What is the ICD-10 code for cystinosis?
The ICD-10-CM code for cystinosis is E72.04. The full clinical description is "Cystinosis". E72.04 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.04 mean?
ICD-10-CM code E72.04 represents “Cystinosis”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and 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.
How does E72.04 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cystinosis affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E72.04?
There is no direct ICD-11 mapping available for E72.04 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.