Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79152
Gene Symbol: FA2H
FA2H
0.120 Biomarker disease BEFREE Fatty acid hydroxylase-associated neurodegeneration due to fatty acid 2-hydroxylase deficiency presents with a wide range of phenotypes including spastic paraplegia, leukodystrophy, and/or brain iron deposition. 22146942 2012
Entrez Id: 79152
Gene Symbol: FA2H
FA2H
0.120 Biomarker disease BEFREE Homozygous mutations in the gene for fatty acid 2-hydroxylase (FA2H) have been associated in humans with three neurodegenerative disorders: complicated spastic paraplegia (SPG35), leukodystrophy with spastic paraparesis and dystonia, and neurodegeneration with brain iron accumulation. 21592092 2011
Entrez Id: 79152
Gene Symbol: FA2H
FA2H
0.120 Biomarker disease HPO
Entrez Id: 79152
Gene Symbol: FA2H
FA2H
0.120 CausalMutation disease CLINVAR