congenital central hypoventilation syndrome

Human disease
rdfs:label
"congenital central hypoventilation syndrome"@en
skos:altLabel
"CCHS"@en
"Ondine curse"@en
"Ondine syndrome"@en
"alveolar hypoventilation secondary to neurologic disease"@en
"central congenital hypoventilation syndrome"@en
"congenital central alveolar hypoventilation syndrome"@en
"congenital central hypoventilation"@en
"idiopathic acquired central hypoventilation syndrome"@en
"primary alveolar hypoventilation"@en
schema:description
"Human disease"@en
schema:dateModified "2026-09-19T08:18:20+00:00"^^xsd:dateTime
schema:version 2547693826
wikibase:identifiers 21
wikibase:sitelinks 20
wikibase:statements 35
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wd:statement/Q979129-C4F50017-317B-4770-871D-4401F2CC8797
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p:P4527 wd:statement/Q979129-07BA9BCC-6D15-4B53-88DD-782D167517C8
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p:P5008 wd:statement/Q979129-BE919292-302A-4F01-8E1D-8D09D3AA1D10
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p:P604 wd:statement/q979129-CD97A84F-E3C4-4A9A-B35D-65CCDC426AA3
p:P6366 wd:statement/Q979129-6A51AAB7-ACE3-49FF-96E3-E76F2F90805D
wd:statement/Q979129-DC0E289B-6714-4E8F-AA5B-E7B3BA40444F
p:P646 wd:statement/Q979129-1453D851-233B-4529-BF6B-61EB92C36DEC
p:P665 wd:statement/Q979129-31BD8F73-DDA1-4E6A-8AD9-B5EF486C4E5B
p:P668 wd:statement/q979129-4BA6A841-A3DF-4B94-9071-C9F55A0C2904
p:P673 wd:statement/q979129-150749C8-FE5A-4C7A-968C-FB8FFF7AAB7F
p:P699 wd:statement/Q979129-74D359A6-040E-43DF-BFC4-5BA294F37DA4
p:direct-normalized/P4527 <http://data.parliament.uk/terms/442287>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C536209>
p:direct-normalized/P6366 <https://makg.org/entity/2910217125>
<https://makg.org/entity/2910467764>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00916>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060731>
wdt:P10283 "C2910106207"
wdt:P11143 "Central hypoventilation syndrome"
wdt:P1550 "661"
"99803"
wdt:P1748 "C98889"
wdt:P1995 neurology
wdt:P2293 PHOX2B
GDNF
ASCL1
wdt:P279 autosomal dominant disease
autonomic nervous system disease
wdt:P2888 <http://identifiers.org/doid/DOID:0060731>
<http://purl.obolibrary.org/obo/DOID_0060731>
<http://www.orpha.net/ORDO/Orphanet_661>
wdt:P2892 "C1275808"
wdt:P31 type of disease
rare disease
wdt:P373 "Central hypoventilation syndrome"
wdt:P4229 "G47.3"
wdt:P4233 "congenital-central-hypoventilation-syndrome"
wdt:P4317 "8535"
wdt:P4527 "442287"
wdt:P486 "C536209"
wdt:P492 "209880"
wdt:P493 "348.8"
wdt:P5008 WikiProject Medicine
wdt:P557 "32976"
wdt:P604 "000078"
wdt:P6366 "2910217125"
"2910467764"
wdt:P646 "/m/03cmv8"
wdt:P665 "H00916"
wdt:P668 "NBK1427"
wdt:P673 "1002927"
wdt:P699 "DOID:0060731"
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