Norrie disease (ND) is a rare X-linked genetic vitreoretinal condition characterized by abnormal retinal development with congenital blindness. Common associated manifestations include sensorineural hearing loss and developmental delay, intellectual disability and/or behavioral disorders. (Orphanet Rare Disease Ontology, Orphanet_649)
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1 genes associated with the disease norrie disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
