sensenbrenner syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050577)
Similar Terms
Downloads & Tools

Genes

3 genes involed in the disease sensenbrenner syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
IFT122 intraflagellar transport 122
WDR19 WD repeat domain 19
WDR35 WD repeat domain 35