| Dataset | HPO Gene-Disease 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://compbio.charite.de/hpoweb/showterm?id=HP:0000667 |
| Similar Terms | |
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3 genes associated with the phthisis bulbi phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
