bietti crystalline corneoretinal dystrophy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050664)
External Link http://www.omim.org/entry/210370
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Genes

1 genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2