E75.21
BillableFabry (-Anderson) disease
Fabry (-Anderson) disease
Coding Notes
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)
- mucolipidosis, types I-III (E77.0-E77.1)
- Refsum's disease (G60.1)
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Alpha-galactosidase A deficiency16652001
- Anderson-Fabry disease16652001
- Angiokeratoma corporis diffusum16652001
- Angiokeratoma corporis diffusum universale16652001
- Cardiovasorenal syndrome16652001
- Ceramide lactoside lipidosis16652001
- Ceramide trihexosidase deficiency16652001
- Fabry disease16652001
- Fabry's disease16652001
- GLA deficiency16652001
- Hereditary dystopic lipidosis16652001
- Lactosyl ceramidosis16652001
- Ruiter-Pompen syndrome16652001
- Sweeley-Klionsky disease16652001
- Thesaurismosis hereditaria16652001
- Thesaurismosis lipoidica16652001
- alpha-Galactosidase-A deficiency16652001
- Deficiency of alpha-galactosidase124464003
- Deficiency of melibiase124464003
- Autonomic neuropathy due to Fabry disease838319005
- Glomerular disease due to Fabry disease1003426008
UMLS
- ALPHA GALACTOSIDASE A DEFIC DISC0002986
- ALPHA-GALACTOSIDASE A DEFICIENCYC0002986
- ANDERSON-FABRY DISEASEC0002986
- Alpha galactosidase A deficiencyC0002986
- Alpha-Galactosidase A DeficiencyC0002986
- Alpha-galactosidase A deficiencyC0002986
- Anderson Fabry DiseaseC0002986
- Anderson-Fabry DiseaseC0002986
- Anderson-Fabry diseaseC0002986
- Angiokeratoma Corporis DiffusumC0002986
- Angiokeratoma DiffuseC0002986
- Angiokeratoma corporis diffusumC0002986
- Angiokeratoma corporis diffusum universaleC0002986
- Angiokeratoma diffuseC0002986
- Angiokeratoma, DiffuseC0002986
- CERAMIDE TRIHEXOSIDASE DEFICIENCYC0002986
- Cardiovasorenal syndromeC0002986
- Ceramide Trihexosidase DeficiencyC0002986
- Ceramide lactoside lipidosisC0002986
- Ceramide trihexosidase deficiencyC0002986
- Deficiency of melibiaseC0002986
- Deficiency, Ceramide TrihexosidaseC0002986
- Deficiency, GLAC0002986
- Deficiency, alpha-Galactosidase AC0002986
- Diffuse AngiokeratomaC0002986
- FABRY DISC0002986
- FABRY DISEASEC0002986
- Fabry (-Anderson) diseaseC0002986
- Fabry DiseaseC0002986
- Fabry diseaseC0002986
- Fabry's DiseaseC0002986
- Fabry's diseaseC0002986
- Fabry's disease (disorder)C0002986
- GLA DEFICIENCYC0002986
- GLA DeficiencyC0002986
- GLA deficiencyC0002986
- HEREDITARY DYSTOPIC LIPIDOSISC0002986
- Hereditary Dystopic LipidosisC0002986
- Hereditary dystopic lipidosisC0002986
- Lactosyl ceramidosisC0002986
- Lipidosis, Hereditary DystopicC0002986
- Ruiter-Pompen syndromeC0002986
- Sweeley-Klionsky diseaseC0002986
- Thesaurismosis hereditariaC0002986
- Thesaurismosis lipoidicaC0002986
- alpha Galactosidase A DeficiencyC0002986
- alpha Galactosidase A Deficiency DiseaseC0002986
- alpha galactosidase deficiencyC0002986
- alpha-Galactosidase A DeficiencyC0002986
- alpha-Galactosidase A Deficiency DiseaseC0002986
- alpha-Galactosidase-A deficiencyC0002986
- anderson-fabry diseaseC0002986
- angiokeratoma corporis diffusumC0002986
- ceramide trihexosidase deficiencyC0002986
- ceramide trihexosidosisC0002986
- disease fabryC0002986
- disease fabry'sC0002986
- fabri diseaseC0002986
- fabry diseaseC0002986
- fabry's diseaseC0002986
- fabrys diseaseC0002986
- thesaurismosis hereditariaC0002986
Frequently Asked Questions
What is the ICD-10 code for fabry (-anderson) disease?
The ICD-10-CM code for fabry (-anderson) disease is E75.21. The full clinical description is "Fabry (-Anderson) disease". E75.21 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E75.21 mean?
ICD-10-CM code E75.21 represents "Fabry (-Anderson) disease". 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 E75.21 a billable code?
Yes, E75.21 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E75.21 in?
E75.21 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E75.21?
E75.21 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 6 more.
What SNOMED CT codes does E75.21 map to?
E75.21 maps to 4 SNOMED CT concepts: 16652001, 838319005, 124464003, 1003426008. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E75.21?
E75.21 is linked to 1 UMLS Concept Unique Identifier: C0002986. 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.