| Dataset | ClinVar Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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). (Orphanet Rare Disease Ontology, Orphanet_779) |
| External Link | http://www.omim.org/entry/613471 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the Reynolds syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| LBR | lamin B receptor |
