brown-vialetto-van laere syndrome 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_0050694)
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Genes

6 genes co-occuring with the disease brown-vialetto-van laere syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3 3.30737
SLC52A1 solute carrier family 52 (riboflavin transporter), member 1 1.99225
UBQLN2 ubiquilin 2 1.17507
UBQLN1 ubiquilin 1 1.17378
NAIP NLR family, apoptosis inhibitory protein 0.869187
C9ORF72 chromosome 9 open reading frame 72 0.699517