Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.250 Biomarker disease BEFREE Multiple parameters were evaluated including: (1) production of GHB (γ-hydroxybutyrate), the biochemical hallmark of SSADHD; (2) rescue from cell death with the dual mTOR (mechanistic target of rapamycin) inhibitor, XL-765, an agent previously shown to rescue aldh5a1-/- mice from premature lethality; (3) mitochondrial number, total reactive oxygen species, and mitochondrial superoxide production, all previously documented as abnormal in aldh5a1-/- mice; (4) total ATP levels and ATP consumption; and (5) selected gene expression profiles associated with epilepsy, a prominent feature in both experimental and human SSADHD. 29053743 2017
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.250 Biomarker disease BEFREE Polymorphisms of ABAT, SCN2A and ALDH5A1 may affect valproic acid responses in the treatment of epilepsy in Chinese. 27918244 2016
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.250 Biomarker disease BEFREE The murine model is a reasonable phenocopy of the human disorder, yet the severity of the seizure disorder in the mouse exceeds that observed in SSADH-deficient patients. 20973619 2011
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.250 Biomarker disease BEFREE Aldh5a1-/-) mouse model suffers from epileptic seizures and succumbs to early lethality. 17457693 2007
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.250 GeneticVariation disease BEFREE The epilepsy that occurs in SSADH deficiency has a seizure phenotype similar to that occurring in the SSADH(-/-) mouse. 16240371 2006
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.250 Biomarker disease MGD