deafness dystonia syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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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Genes

1 genes involed in the disease deafness dystonia syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

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