| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | congenital defect of the optic nerve in which some part of the structure is absent (Mammalian Phenotype Ontology, MP_0010717) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010717 |
| Similar Terms | |
| Downloads & Tools |
3 gene mutations causing the optic nerve coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
