| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A scotoma (area of diminished vision within the visual field) located between the central point of fixation and the blind spot with a roughly horizontal oval shape. (Human Phenotype Ontology, HP_0000576) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0000576 |
| Similar Terms | |
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1 genes associated with the centrocecal scotoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| OPA1 | optic atrophy 1 (autosomal dominant) |
