| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A mitochondrial metabolism disease that is characterized by hearing loss that begins early in life, problems with movement, impaired vision, and behavior problems. (Human Disease Ontology, DOID_0050757) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C535808 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Mohr-Tranebjaerg 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 |
