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)
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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