Mohr-Tranebjaerg syndrome Gene Set

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

Genes

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