|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of one of the photoreceptor cell types in the retina, in which the photopigment is in invaginations of the cell membrane of the outer segment (Mammalian Phenotype Ontology, MP_0008447)|
|Downloads & Tools|
2 gene mutations causing the absent retinal cone cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.