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Reynolds syndrome

Synonyms
PRIMARY BILIARY CIRRHOSIS, SCLERODERMA, RAYNAUD DISEASE, AND TELANGIECTASIA
Modes of inheritance
Not genetically inherited (Orphanet)

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.

Clinical tests (19 available)

Molecular Genetics 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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Imported from Human Phenotype Ontology (HPO)

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