ohtahara syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A neonatoal period electroclinical syndrome that is characterized by tonic spasms and partial seizures. (Human Disease Ontology, DOID_0050709)
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Genes

2 genes involed in the disease ohtahara syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ARX aristaless related homeobox
CDKL5 cyclin-dependent kinase-like 5