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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Central hypoventilation syndrome, congenital
Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction
Identifiers
MONDO:0030537
OMIM:619482
Part of
Central hypoventilation syndrome, congenital
Also known as
CCHS2
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