| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A communication disorder that is a loss of ability to recognize objects, persons, sounds, shapes, or smells while the specific sense is not defective nor is there any significant memory loss. (Human Disease Ontology, DOID_4090) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0010524 |
| Similar Terms | |
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8 genes associated with the agnosia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GRIN2A | glutamate receptor, ionotropic, N-methyl D-aspartate 2A |
| MLH1 | mutL homolog 1 |
| MSH2 | mutS homolog 2 |
| MSH6 | mutS homolog 6 |
| PMS2 | PMS2 postmeiotic segregation increased 2 (S. cerevisiae) |
| PSEN1 | presenilin 1 |
| TREM2 | triggering receptor expressed on myeloid cells 2 |
| TYROBP | TYRO protein tyrosine kinase binding protein |
