SHMARQL

hemophilia B

<http://www.wikidata.org/entity/Q2562598>

inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait
rdfs:label
"hemophilia B"@en
skos:altLabel
"Christmas disease"@en
"Congenital factor IX deficiency"@en
"Congenital factor IX disorder"@en
"Factor IX deficiency"@en
"Hemophilia B (disorder)"@en
"deficiency, functional factor IX"@en
"factor IX deficiency"@en
"haemophilia B"@en
schema:description
"inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait"@en
schema:dateModified "2026-10-24T00:51:45+00:00"^^xsd:dateTime
schema:version 2560169539
wikibase:identifiers 34
36
wikibase:sitelinks 16
wikibase:statements 55
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p:P9863 wd:statement/Q2562598-f1506872-43fb-46bf-b0dc-643878d4b70a
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D002836>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010604>
p:direct-normalized/P6366 <https://makg.org/entity/2777081929>
<https://makg.org/entity/2909704213>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C15.378.100.100.510>
<http://id.nlm.nih.gov/mesh/C15.378.100.141.510>
<http://id.nlm.nih.gov/mesh/C15.378.463.510>
<http://id.nlm.nih.gov/mesh/C16.320.099.510>
<http://id.nlm.nih.gov/mesh/C16.320.322.235>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:12259>
p:direct-normalized/P8814 <http://wordnet-rdf.princeton.edu/rdf/id/14194469-n>
wdt:P10283 "C2777081929"
wdt:P10376 "nursing-and-health-professions/hemophilia-b"
wdt:P11143 "Haemophilia B"
wdt:P11430 "DI-02248"
wdt:P1193 0.00005^^xsd:decimal
wdt:P1199 X-linked recessive
wdt:P13204 "byr8k2gv"
wdt:P1417 "science/hemophilia-B"
wdt:P1461 "haemophilia-b-factor-ix-deficiency"
wdt:P14914 "D98879"
wdt:P1550 "98879"
wdt:P1692 "286.1"
wdt:P1748 "C26721"
wdt:P1995 hematology
wdt:P2293 F9
wdt:P279 inherited blood coagulation disease
coagulation factor deficiency
X-linked recessive disease
wdt:P2841 neonatal onset
infantile onset
childhood onset
wdt:P2888 <http://identifiers.org/doid/DOID:12259>
<http://purl.obolibrary.org/obo/DOID_12259>
wdt:P2892 "C0008533"
wdt:P31 type of disease
wdt:P3417 "Hemophilia-B"
wdt:P373 "Hemophilia B"
wdt:P3827 "hemophilia-b"
wdt:P4229 "D67"
wdt:P4233 "hemophilia-b"
wdt:P4317 "8732"
wdt:P486 "D002836"
wdt:P492 "306900"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010604"
wdt:P557 "5561"
wdt:P604 "000539"
wdt:P6366 "2777081929"
"2909704213"
wdt:P646 "/m/01cbkb"
wdt:P6532 Spontaneous, recurrent epistaxis
cephalohematoma
intracranial hemorrhage
wdt:P672 "C15.378.100.100.510"
"C15.378.100.141.510"
"C15.378.463.510"
"C16.320.099.510"
"C16.320.322.235"
wdt:P673 "779434"
wdt:P699 "DOID:12259"
wdt:P7329 "3B11.0"
wdt:P7807 "1901375668"
wdt:P8814 "14194469-n"
wdt:P9272 "2885"
wdt:P9863 "રુધિરસ્રાવિતા-નવમઘટકીય"
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