|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||reduced likelihood that an organism will develop disease symptoms similar to human sight-threatening inflammatory eye diseases upon induction by peripheral immunization with one of several uveitogenic retinal proteins (or with peptides derived from them), or by the adoptive transfer of lymphocytes specific to these antigens (Mammalian Phenotype Ontology, MP_0004822)|
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4 gene mutations causing the decreased susceptibility to experimental autoimmune uveoretinitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.