rdfs: label
en
fr
"Haddad syndrome"@en
"syndrome de Haddad"@fr
skos: altLabel
"Congenital central alveolar hypoventilation-Hirschsprung disease syndrome"@en
"Ondine-Hirschsprung disease"@en
"Ondine-Hirschsprung syndrome"@en
schema: 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)"@en
schema: dateModified
"2024-02-26T20:59:51+00:00"^^xsd:dateTime
schema: version
2088124834
wikibase: identifiers
6
wikibase: sitelinks
0
wikibase: statements
11
p: P1550
wd: statement/Q56014441-C04B7124-9E58-4F68-B84C-F2B77F27E859
p: P2293
wd: statement/Q56014441-1A02FE74-4B94-4A60-BDC6-E419441D507E
p: P279
wd: statement/Q56014441-4d5e3ccc-4566-6446-5e88-0a0f4eb47dc0
wd: statement/Q56014441-91d92dc6-4fec-3c4d-b58b-756f7f166e6b
p: P2888
wd: statement/Q56014441-FFF08A05-E4F0-46CA-A09A-6AA7E004C6E5
p: P2892
wd: statement/Q56014441-3105B2EF-8954-497D-B51F-E5FE796EFB48
wd: statement/Q56014441-9F203CFC-4134-4AC7-A1F7-CECEE74364E4
p: P31
wd: statement/Q56014441-6F3AD674-9843-4CA1-B9CE-32A48E08B8B0
p: P4229
wd: statement/Q56014441-CFBA865B-79FC-4A00-BD6A-A00BE6CF9BE5
p: P486
wd: statement/Q56014441-AD1309F9-EF46-43F1-8E3E-BF84FFC8FA8F
p: P5270
wd: statement/Q56014441-A1BA95C2-EEF8-46F0-9083-654504B3050E
p: direct-normalized/P486
<http://id.nlm.nih.gov/mesh/C536209>
p: direct-normalized/P5270
<http://purl.obolibrary.org/obo/MONDO_0020493>
wdt: P1550
"99803"
wdt: P2293
PHOX2B
wdt: P279
Hirschsprung's disease
congenital central hypoventilation syndrome
wdt: P2888
<http://www.orpha.net/ORDO/Orphanet_99803>
wdt: P2892
"C1859049"
"C1859587"
wdt: P31
type of disease
wdt: P4229
"G47.3"
wdt: P486
"C536209"
wdt: P5270
"MONDO_0020493"