Farber disease (Q53203): Difference between revisions
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13 August 2026
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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. |
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CID11:ID_122136943
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dki-india-ID_122136943
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Concluído
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13 August 2026
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