Fabry disease (Q40070): Difference between revisions
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A doença de Fabry é uma doença de depósito lisossomal multissistêmica progressiva, hereditária, caracterizada por manifestações neurológicas, cutâneas, renais, cardiovasculares, cócleo-vestibulares e cerebrovasculares. | |||
| description / en | description / en | ||
Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterised by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations. | |||
Revision as of 05:44, 13 August 2026
Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterised by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C56.01 |
||
| English | Fabry disease |
Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterised by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations. |
