Gene: LCAT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3931
Gene Symbol: LCAT
LCAT 		0.110 GeneticVariation disease BEFREE The gene encoding for LCAT has been mapped to chromosome 16q22.1, and several mutations of this gene cause LCAT deficiency which is inherited as an autosomal recessive trait and which is characterized by corneal opacities, normochromic normocytic anemia, and renal dysfunction. 11423760 2001
Entrez Id: 3931
Gene Symbol: LCAT
LCAT 		0.110 Biomarker disease HPO