Gene: FA2H ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79152
Gene Symbol: FA2H
FA2H 		0.010 GeneticVariation disease BEFREE Rare recessive causes include PLA2G6 mutations (infantile neuroaxonal dystrophy), and mutations of ATP13A2 (Kufor Rakeb syndrome) and FA2H. 22515743 2012