1.2.1.31 Acidosis, Lactic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22529283&form=6&db=m Profound neonatal hypoglycemia and lactic acidosis caused by pyridoxine-dependent epilepsy. causal interaction,unassigned 4,0 1.2.1.31 Adenocarcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33537098&form=6&db=m Overall survival of pancreatic ductal adenocarcinoma is doubled by Aldh7a1 deletion in the KPC mouse. causal interaction,diagnostic usage,ongoing research,therapeutic application 4,3,4,1 1.2.1.31 Arthritis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15331127&form=6&db=m The importance of timing of adrenergic drug delivery in relation to the induction and onset of adjuvant-induced arthritis. diagnostic usage,ongoing research,unassigned 2,3,0 1.2.1.31 Asthma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6254580&form=6&db=m Prostaglandins, steroids and reception (an attempt to model the structure of the active centers of adrenoreception). unassigned - 1.2.1.31 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17721876&form=6&db=m An intriguing "silent" mutation and a founder effect in antiquitin (ALDH7A1). causal interaction,unassigned 4,0 1.2.1.31 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21704546&form=6&db=m Pyridoxine dependent epilepsy and antiquitin deficiency Clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up. causal interaction,diagnostic usage,therapeutic application,unassigned 4,2,3,0 1.2.1.31 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25818041&form=6&db=m Diagnostic yield of genetic testing in epileptic encephalopathy in childhood. causal interaction,unassigned 4,0 1.2.1.31 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26995068&form=6&db=m Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum. causal interaction,diagnostic usage,unassigned 4,3,0 1.2.1.31 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27342130&form=6&db=m The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies. causal interaction,diagnostic usage,unassigned 3,3,0 1.2.1.31 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30005813&form=6&db=m Brain malformations associated to Aldh7a1 gene mutations: Report of a novel homozygous mutation and literature review. causal interaction,unassigned 3,0