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GTR Home > Conditions/Phenotypes > Reynolds syndrome

Summary

An autoimmune disorder characterized by the association of primary biliary cirrhosis with limited cutaneous systemic sclerosis. Onset occurs between 30-65 years. Occurs sporadically, but rare familial cases with an unknown inheritance pattern have been observed. There is no cure and management is mainly supportive. [from SNOMEDCT_US]

Available tests

19 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: C14SR, DHCR14B, LMN2R, PHA, PHASK, TDRD18, LBR
    Summary: lamin B receptor

Clinical features

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