|
OMIM:209880 - CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS
DOID:0060731 - congenital central hypoventilation syndrome |
MONDO:0008852 - congenital central hypoventilation syndrome |
Human Disease Resources: OMIM
Xenbase Genes: gdnf, ret, phox2b, ascl1, bdnf, edn3