Gyrate Atrophy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping by NeuroDevNet. [LS]. (Human Disease Ontology, DOID_1415)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D015799
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Genes

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

Symbol Name Standardized Value
OAT ornithine aminotransferase 2.88009