| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Atrophy of the eyeball with blindness and decreased intraocular pressure due to end-stage intraocular disease. (Human Phenotype Ontology, HP_0000667) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006249 |
| Similar Terms | |
| Downloads & Tools |
1 gene mutations causing the phthisis bulbi phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| SH3PXD2B | SH3 and PX domains 2B |
