learning disability Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A specific developmental disorder that involves difficulty in scholastic skills such as reading, writing, spelling, reasoning, recalling and/or organizing information resulting from the brain's inability to receive and process information. (Human Disease Ontology, DOID_8927)
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Genes

3 genes associated with the disease learning disability in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PCSK6 proprotein convertase subtilisin/kexin type 6 0.486425
CTSO cathepsin O 0.438544
GLRX3 glutaredoxin 3 0.064973