Haddad syndrome (Q94162)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1685926536 |
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| English | Haddad syndrome |
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. |
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CID11:ID_1685926536
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dki-india-ID_1685926536
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