|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the fibrous, outer envelope of the eyeball, covering it entirely excepting the segment covered anteriorly by the cornea (Mammalian Phenotype Ontology, MP_0010710)|
|Downloads & Tools|
1 gene mutations causing the absent sclera phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|RXRA||retinoid X receptor, alpha|