Term info
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/3898
created by
https://orcid.org/0000-0001-5208-3432
definition
Any inherited retinal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.
has exact synonym
retinopathy caused by mutation in GUCY2D
id
MONDO:0100454