Basal Laminar Drusen Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2569)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C563034
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Genes

1 genes/proteins associated with the disease Basal Laminar Drusen from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CFH complement factor H 2.88009