DEAFNESS, AUTOSOMAL RECESSIVE 18A Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:602092
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Genes

1 genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 18A from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
USH1C Usher syndrome 1C (autosomal recessive, severe) 2.88009