Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C1858080
Disease: Retinal Dystrophy, Early Onset Severe
Retinal Dystrophy, Early Onset Severe 		0.320 GermlineCausalMutation ORPHANET Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study. 22570351

2012