Stargardt disease 1 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C535804
Similar Terms
Downloads & Tools

Genes

2 genes/proteins associated with the disease Stargardt disease 1 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CNGB3 cyclic nucleotide gated channel beta 3 2.88009
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 2.88009