Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.710 GermlineCausalMutation ORPHANET Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays. 18055821

2007