retinal degeneration, late-onset, autosomal dominant Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/605670
Similar Terms
Downloads & Tools

Genes

1 genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
C1QTNF5 C1q and tumor necrosis factor related protein 5