Oculocerebrorenal Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1056)
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Genes

2 genes associated with the Oculocerebrorenal Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CLCN5 chloride channel, voltage-sensitive 5
TMEM27 transmembrane protein 27