Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5959
Gene Symbol: RDH5
RDH5
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		0.010 GeneticVariation BEFREE One patient had compound heterozygous mutations in RDH5 and suffered from FAP with mild maculopathy. 22559933

2012