door syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description DOORS syndrome (also known as DOOR syndrome) is a multiple congenital anomalies-intellectual disability syndrome characterized by sensorineural hearing loss (deafness), onychodystrophy, osteodystrophy, mild to profound intellectual disability, and seizures. (Orphanet Rare Disease Ontology, Orphanet_79500)
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1 genes associated with the door syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TBC1D24 TBC1 domain family, member 24