Haddad syndrome

Preferred Label : Haddad syndrome;

ICD-11 definition : Haddad syndrome is a rare genetic congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Intestinal aganglionosis is more extensive than in classical Hirschsprung disease.;

Details

Origin ID

1685926536;

Automatic exact mappings (from CISMeF team)
- Central hypoventilation syndrome, congenital, 1 [OMIM Phenotype]
- Haddad syndrome [ORDO Disease]
- Haddad syndrome (disorder) [SNOMED CT concept]
- congenital central hypoventilation syndrome [MeSH Supplementary Concept]

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