| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/311150 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the jensen syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TIMM8A | translocase of inner mitochondrial membrane 8 homolog A (yeast) |
