deafness dystonia syndrome Gene Set

Dataset DISEASES Text-mining 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

12 genes co-occuring with the disease deafness dystonia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast) 2.33446
TIMM13 translocase of inner mitochondrial membrane 13 homolog (yeast) 1.93702
ANO3 anoctamin 3 1.67548
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type 1.58715
CIZ1 CDKN1A interacting zinc finger protein 1 1.56978
DCAF17 DDB1 and CUL4 associated factor 17 1.49964
THAP1 THAP domain containing, apoptosis associated protein 1 1.32236
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide 1.29178
GCH1 GTP cyclohydrolase 1 1.26429
ALS2 amyotrophic lateral sclerosis 2 (juvenile) 1.12277
TIMM23 translocase of inner mitochondrial membrane 23 homolog (yeast) 1.00246
BTK Bruton agammaglobulinemia tyrosine kinase 0.626103