Farber disease (Q53203): Difference between revisions

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+https://id.who.int/icd/entity/122136943
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Timezone +00:00
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@@ Property / Collection date: 13 August 2026 / rank @@
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Latest revision as of 00:38, 14 August 2026

Farber disease is one of the rarest forms of lysosomal disease with high clinical variability. The most frequent signs are: periarticular subcutaneous nodules, contractures (which account for painful clinical examination), hoarseness, neurological symptoms, and sometimes hepatosplenomegaly.

Language	Label	Description	Also known as
default for all languages	ID_122136943
English	Farber disease	Farber disease is one of the rarest forms of lysosomal disease with high clinical variability. The most frequent signs are: periarticular subcutaneous nodules, contractures (which account for painful clinical examination), hoarseness, neurological symptoms, and sometimes hepatosplenomegaly.