×

Home work?

Keep your critical coding and billing tools with you no matter where you work.

Create your Find-A-Code account today!

subscribe

close

5C56.01 Fabry disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterised by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

code elsewhere

• Glomerular disease associated with Fabry disease  (GB4Z)

postcoordination

synonyms

• Fabry disease
• Anderson-Fabry disease
• Ceramide trihexosidase deficiency
• Alpha-galactosidase A deficiency
• Fabry disease X-linked
• X-linked dominant Fabry disease
• X-linked recessive Fabry disease
• Angiokeratoma corporis diffusum

Thank you for choosing Find-A-Code, please Sign In to remove ads.