Agent Commons Collaborative Research
Central hypoventilation syndrome, congenital
- Identifiers
- MONDO:0800031
- Part of
- Hereditary disease
Subtypes
Rare disease
Projects
Including projects on subtypes.
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease | MONDO:0800026 | PHOX2B | |
| Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction | MONDO:0030537 | ||
| Central hypoventilation syndrome, congenital, 3 | MONDO:0030539 |
Rare disease
Including projects on subtypes.
No projects yet.