Belgian Genetic Tests database
Reynolds syndrome
| Name: |
Reynolds syndrome
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| Description: |
Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc) (see these terms).
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| ORPHAcode: |
779
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| Synonyms: |
Primary biliary cirrhosis and systemic scleroderma
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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