1. Diseases
  2. Haddad syndrome

Haddad syndrome

Disease Export to PDF
Name:
Haddad syndrome
Description:
Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease (see these terms).
ORPHAcode:
99803
Synonyms:
Congenital central alveolar hypoventilation-Hirschsprung disease syndrome
Ondine-Hirschsprung disease
Ondine-Hirschsprung syndrome
XREF(s):
Orphanet
ICD-10
MeSH
OMIM
Analyte(s):
PHOX2B
RET
ASCL1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14