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
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
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
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