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Summary Literature (1)
OMIM:209880 - CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS


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

In Mondo Disease Ontology:
MONDO:0008852 - congenital central hypoventilation syndrome

Human Disease Resources: OMIM

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