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Summary Literature (1)
MIM:209880 - CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 1; CCHS1

Xenbase Genes: gdnf, ret, phox2b, ascl1, bdnf, edn3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008852 - obsolete congenital central hypoventilation syndrome
MONDO:0020493 - Haddad syndrome
MONDO:0800026 - central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease

Disease Ontology (DO):
DOID:0060731 - congenital central hypoventilation syndrome