biotin-responsive basal ganglia disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050659)
Similar Terms
Downloads & Tools

Genes

9 genes co-occuring with the disease biotin-responsive basal ganglia disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC19A3 solute carrier family 19 (thiamine transporter), member 3 2.78248
SLC5A6 solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6 1.70406
SLC19A1 solute carrier family 19 (folate transporter), member 1 1.59206
SLC19A2 solute carrier family 19 (thiamine transporter), member 2 1.53921
SLC46A1 solute carrier family 46 (folate transporter), member 1 1.28304
FOLR2 folate receptor 2 (fetal) 1.0837
FOLR1 folate receptor 1 (adult) 1.01047
BTD biotinidase 0.984743
GCH1 GTP cyclohydrolase 1 0.813462