central hypoventilation syndrome, congenital, with or without hirschsprung disease 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

1 genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PHOX2B paired-like homeobox 2b