mohr-tranebjaerg syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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 associated with the mohr-tranebjaerg syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)