Jensen syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A syndrome that is characterized by sensorineural hearing loss with onset in infancy, followed in adolescence by progressive optic nerve atrophy with loss of vision and in adulthood by progressive dementia. (Human Disease Ontology, DOID_0050867)
External Link http://www.omim.org/entry/311150
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Genes

1 genes associated with the Jensen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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