townes-brocks syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease that is characterized by imperforate anus, dysplastic ears often associated with sensorineural and/or conductive hearing impairment, and thumb malformations. (Human Disease Ontology, DOID_0050887)
External Link http://www.omim.org/entry/107480
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Genes

1 genes associated with the townes-brocks syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SALL1 spalt-like transcription factor 1