Coloboma Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An eye disease characterized by missing pieces of tissue in structures that form the eye, such as the iris, retina, choroid or optic disc. (Human Disease Ontology, DOID_12270)
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7 genes/proteins associated with the disease Coloboma from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LAMB1 laminin, beta 1 2.88009
ACTB actin, beta 2.88009
SHH sonic hedgehog 2.88009
PAX6 paired box 6 2.88009
ACTG1 actin gamma 1 2.88009
ALDH7A1 aldehyde dehydrogenase 7 family, member A1 2.88009
GDF6 growth differentiation factor 6 2.88009