central hypoventilation syndrome, congenital Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/209880
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Genes

4 genes associated with the central hypoventilation syndrome, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
BDNF brain-derived neurotrophic factor
EDN3 endothelin 3
RET ret proto-oncogene