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Haddad syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0020493

Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. [ Orphanet:99803 ]

Synonyms: ondine-Hirschsprung disease Haddad syndrome congenital central alveolar hypoventilation-Hirschsprung disease syndrome ondine-Hirschsprung syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:99803 (MONDO:equivalentTo)
  • ICD10CM:G47.3 (Orphanet:99803/ntbt)
  • GARD:16909 (Orphanet:99803)
  • SCTID:719972004 (MONDO:equivalentTo)
Subsets

gard_rare, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare, clingen

exactMatch

http://identifiers.org/snomedct/719972004

http://www.orpha.net/ORDO/Orphanet_99803

id

MONDO:0020493

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0020493

Term relations