Gene: ACMSD ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 130013
Gene Symbol: ACMSD
ACMSD 		0.020 GeneticVariation group BEFREE Further support for this comes from the recent identification of a disease-segregating stop codon mutation in ACMSD in a family with Parkinsonism, and a missense mutation in the ACMSD gene predicted to disrupt enzyme function in an individual with typical PD. 29103054 2017
Entrez Id: 130013
Gene Symbol: ACMSD
ACMSD 		0.020 GeneticVariation group BEFREE ACMSD is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism. 23955123 2013