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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 15-07-2010 |
Symbol | RS | ||
Location | 1q42.12 | ||
Name | Reynolds syndrome | ||
Other name(s) | primary biliary cirrhosis, scleroderma, Raynaud disease, and telangiectasia | ||
Corresponding gene | LBR | ||
related resource | Retinal Information Network | ||
Main clinical features |
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Genetic determination
Function/system disorder
| Type
| disease
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Remark(s) |