SHMARQL

congenital hyperinsulinism

<http://www.wikidata.org/entity/Q5160437>

genetic disease
rdfs:label
"congenital hyperinsulinism"@en
skos:altLabel
"CHI"@en
"PHHI"@en
"Persistent hyperinsulinemic hypoglycemia of infancy"@en
schema:description
"genetic disease"@en
schema:dateModified "2026-10-24T00:29:38+00:00"^^xsd:dateTime
schema:version 2560166288
wikibase:identifiers 19
22
wikibase:sitelinks 11
wikibase:statements 43
p:P10283 wd:statement/Q5160437-BB8C15E3-E395-4A4C-9A7A-8566E13BF2CE
p:P14914 wd:statement/Q5160437-37E0796F-4BE3-4C75-A60F-D481C2BD8BE9
p:P1550 wd:statement/Q5160437-16B84D51-2AAB-4595-95D2-7FD666D88167
p:P1748 wd:statement/Q5160437-38E0183C-95E6-43D5-8800-CCD05B6B065C
wd:statement/Q5160437-e5d98ee9-4892-4a87-d6e3-152bf2e18ec7
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wd:statement/Q5160437-7E55D119-0CB5-419F-AC22-92263B35163B
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wd:statement/Q5160437-E7A23ABD-897E-440A-BB54-20135F625A6B
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p:P492 wd:statement/Q5160437-FD075B41-0DC1-4FFB-A6EC-E5047055F34C
p:P5270 wd:statement/Q5160437-81BCD0E1-581D-4F33-9282-F375AE6F3AD9
p:P6366 wd:statement/Q5160437-0AAA0095-9069-4690-9D67-0C2C2C283C79
p:P646 wd:statement/Q5160437-55754879-85C5-4188-A974-5A05243E9BCA
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wd:statement/Q5160437-77B43C94-61EF-44CC-B90E-422B12DD2B89
wd:statement/Q5160437-EABE094B-611F-4C98-BF89-2A38600F60CB
p:P7464 wd:statement/Q5160437-9A73B7A5-4732-450F-80D6-58B69FDA0F8D
p:P9272 wd:statement/Q5160437-DC98DF37-AB70-4337-9D10-E92E184840B4
p:direct-normalized/P2581 <http://babelnet.org/rdf/s00497498n>
p:direct-normalized/P4527 <http://data.parliament.uk/terms/512659>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D044903>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0019010>
p:direct-normalized/P6366 <https://makg.org/entity/2777643638>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C06.689.150>
<http://id.nlm.nih.gov/mesh/C16.614.200>
<http://id.nlm.nih.gov/mesh/C18.452.394.968.250>
<http://id.nlm.nih.gov/mesh/C18.452.394.984.200>
wdt:P10283 "C2777643638"
wdt:P14914 "D00657"
wdt:P1550 "657"
wdt:P1748 "C122923"
"C131425"
wdt:P1995 gastroenterology
pediatrics
endocrinology
wdt:P2293 GCK
GLUD1
KCNJ11
HADH
HNF4A
SLC16A1
ABCC8
HNF1A
UCP2
wdt:P2581 "00497498n"
wdt:P279 hypoglycemia
hyperinsulinism
genetic pancreatic disease
wdt:P2841 neonatal onset
infantile onset
childhood onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_657>
wdt:P2892 "C0027773"
"C1257959"
"C3888018"
wdt:P31 type of disease
wdt:P4229 "E16.1"
wdt:P4527 "512659"
wdt:P486 "D044903"
wdt:P492 "256450"
wdt:P5270 "MONDO_0019010"
wdt:P6366 "2777643638"
wdt:P646 "/m/04rm1q"
wdt:P672 "C06.689.150"
"C16.614.200"
"C18.452.394.968.250"
"C18.452.394.984.200"
wdt:P7464 "congenital-hyperinsulinism"
wdt:P9272 "38055"
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data from SPARQL profile: Wikidata