congenital central hypoventilation syndrome

Preferred Label : congenital central hypoventilation syndrome;

MeSH note : PROM;

CISMeF synonym : cchs with hirschsprung disease;

MeSH synonym : congenital ondine curse; primary alveolar hypoventilation; congenital failure of autonomic control; idiopathic congenital central alveolar hypoventilation; ondine curse, congenital; autonomic control, congenital failure of; central hypoventilation syndrome, congenital;

Related MeSH term : Ondine-Hirschsprung Disease; Haddad Syndrome;

Détails

Origin ID

C536209;

UMLS CUI

C1275808;

Automatic exact mappings (from CISMeF team)
- Congenital central alveolar sleep-related hypoventilation [ICD-11 Subcategory]
- Haddad syndrome [ICD-11 More detail]
- Primary alveolar hypoventilation [ICD-11 More detail]
- Primary alveolar hypoventilation (finding) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Central hypoventilation syndrome, congenital [OMIM phenotypic series]
- Central hypoventilation syndrome, congenital, 1 [OMIM Phenotype]
- Congenital Central Hypoventilation [NCIt concept]
- Congenital central alveolar hypoventilation syndrome [ICD-9 code]
- Congenital central hypoventilation (disorder) [SNOMED CT concept]
- Congenital central hypoventilation syndrome [ORDO Disease]
- Congenital central hypoventilation syndrome [MedDRA Preferred Term]
- Haddad syndrome [ORDO Disease]
- Haddad syndrome (disorder) [SNOMED CT concept]
- Sleep-related respiratory failure (disorder) [SNOMED CT concept]
- congenital central hypoventilation syndrome [DO Concept]
- congenital central hypoventilation syndrome [Disease (Nov.)]
- primary alveolar hypoventilation [SNOMED Notion]
DO Cross reference
- congenital central hypoventilation syndrome [DO Concept]
MeSH term(s) associated for indexing
- hypoventilation [MeSH Descriptor]
- sleep apnea, central [MeSH Descriptor]
ORDO relation(s)
- Haddad syndrome [ORDO Disease]
Record concept(s)
- Congenital central hypoventilation syndrome [MeSH concept]
- cchs with hirschsprung disease [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Central hypoventilation syndrome, congenital, 1 [OMIM Phenotype]
- Congenital Central Hypoventilation [NCIt concept]
- Congenital central alveolar hypoventilation syndrome [ICD-9 code]
- Congenital central hypoventilation (disorder) [SNOMED CT concept]
- Congenital central hypoventilation syndrome [MedDRA Preferred Term]
- Congenital central hypoventilation syndrome [ORDO Disease]
- Haddad syndrome [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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