Gene: PLPBP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11212
Gene Symbol: PLPBP
PLPBP 		0.110 GeneticVariation group BEFREE Suspected clinical diagnoses prior to identification of PLPBP variants included mitochondrial encephalopathy (two patients), folinic acid-responsive epilepsy (one patient) and a movement disorder compatible with AADC deficiency (one patient). 30668673 2019
Entrez Id: 11212
Gene Symbol: PLPBP
PLPBP 		0.110 Biomarker group HPO