Haddad syndrome (Q94162): Difference between revisions
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Revision as of 09:17, 16 August 2026
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 |
||
| 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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