| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A syndrome that is characterized by sensorineural hearing loss with onset in infancy, followed in adolescence by progressive optic nerve atrophy with loss of vision and in adulthood by progressive dementia. (Human Disease Ontology, DOID_0050867) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537568 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Jensen syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TIMM8A | translocase of inner mitochondrial membrane 8 homolog A (yeast) | 2.88009 |
