Stargardt disease 1 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness. (Human Disease Ontology, DOID_0050817)
External Link http://www.omim.org/entry/248200
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Genes

2 genes associated with the Stargardt disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
CNGB3 cyclic nucleotide gated channel beta 3