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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •mucolipidosis, types I-IIIE77.0-E77.1
- •Refsum's diseaseG60.1
- •adrenoleukodystrophy [Addison-Schilder]E71.528
Related Codes(8)
Also Known As / Clinical Terms(124)
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
Clinical Terms
- fabrys disease
- Alpha-Galactosidase A Deficiency
- Fabry's Disease
- Lipidosis, Hereditary Dystopic
- Sweeley-Klionsky disease
- Anderson-Fabry Disease
- ceramide trihexosidase deficiency
- ceramide trihexosidosis
- Deficiency, alpha-Galactosidase A
- GLA deficiency
- FABRY DIS
- Cardiovasorenal syndrome
- Angiokeratoma corporis diffusum
- Fabry's disease (disorder)
- fabry disease
- Autonomic neuropathy due to Fabry disease
- Deficiency of alpha-galactosidase
- HEREDITARY DYSTOPIC LIPIDOSIS
- alpha-Galactosidase A Deficiency Disease
- thesaurismosis hereditaria
- Thesaurismosis lipoidica
- Deficiency, GLA
- disease fabry
- alpha Galactosidase A Deficiency Disease
- Lactosyl ceramidosis
- fabri disease
- Angiokeratoma, Diffuse
- alpha Galactosidase A Deficiency
- Ceramide lactoside lipidosis
- Diffuse Angiokeratoma
- disease fabry's
- Ruiter-Pompen syndrome
- Angiokeratoma Diffuse
- Anderson Fabry Disease
- alpha galactosidase deficiency
- Angiokeratoma corporis diffusum universale
- Deficiency of melibiase
- Glomerular disease due to Fabry disease
- ALPHA GALACTOSIDASE A DEFIC DIS
- alpha-Galactosidase-A deficiency
- Deficiency, Ceramide Trihexosidase
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.
How does E75.21 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like fabry (-anderson) disease 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 E75.21?
There is no direct ICD-11 mapping available for E75.21 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.