Central hypoventilation syndrome, congenital - CISMeF

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CISMeF

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Central hypoventilation syndrome, congenitalOMIM phenotypic series

Preferred Label : Central hypoventilation syndrome, congenital;

Details

Origin ID

PS209880;

Currated CISMeF NLP mapping
- Congenital Central Hypoventilation [NCIt concept]
- Congenital central hypoventilation syndrome [ORDO Disease]
- Congenital central hypoventilation syndrome [MeSH concept]
- Congenital central hypoventilation syndrome [MedDRA Preferred Term]
- congenital central hypoventilation syndrome [DO Concept]
- congenital central hypoventilation syndrome [MeSH Supplementary Concept]
- sleep apnea, central [MeSH Descriptor]
Validated automatic mappings to BTNT
- Congenital central alveolar sleep-related hypoventilation [ICD-11 Subcategory]

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25/05/2024

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