hypoprothrombinemia

Human disease
rdfs:label
"hypoprothrombinemia"@en
skos:altLabel
"Congenital factor II deficiency"@en
"Dysprothrombinemia"@en
"Factor 2 deficiency"@en
"Factor II deficiency"@en
"PROTHROMBIN DEFICIENCY, CONGENITAL"@en
"prothrombin deficiency"@en
schema:description
"Human disease"@en
schema:dateModified "2026-10-24T00:07:10+00:00"^^xsd:dateTime
schema:version 2560162626
wikibase:identifiers 27
30
wikibase:sitelinks 5
wikibase:statements 58
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p:direct-normalized/P3201 <http://purl.bioontology.org/ontology/MDRFRE/10063563>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D007020>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0013361>
p:direct-normalized/P6366 <https://makg.org/entity/2777260480>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H01254>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C15.378.100.100.550>
<http://id.nlm.nih.gov/mesh/C15.378.100.141.550>
<http://id.nlm.nih.gov/mesh/C15.378.463.550>
<http://id.nlm.nih.gov/mesh/C16.320.099.550>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:2235>
wdt:P10283 "C2777260480"
wdt:P11430 "DI-02664"
wdt:P1193 0.000001^^xsd:decimal
wdt:P13204 "geymdj2w"
wdt:P1417 "science/hypoprothrombinemia"
wdt:P14914 "D00325"
wdt:P1550 "325"
wdt:P1692 "286.3"
wdt:P1748 "C131737"
"C26799"
wdt:P1995 hematology
wdt:P2176 menadiol
menadione
wdt:P2293 F2
wdt:P279 autosomal recessive disease
thrombophilia
reduced prothrombin activity
congenital vitamin K-dependent coagulation factors deficiency
wdt:P2841 any age
wdt:P2888 <http://identifiers.org/doid/DOID:2235>
<http://purl.obolibrary.org/obo/DOID_2235>
<http://www.orpha.net/ORDO/Orphanet_325>
wdt:P2892 "C0020640"
"C0272317"
"C3203356"
"C4722227"
wdt:P31 type of disease
rare disease
wdt:P3201 "10063563"
wdt:P3827 "hypoprothrombinemias"
wdt:P4229 "D68.2"
wdt:P4233 "prothrombin-deficiency"
wdt:P4317 "2235"
wdt:P486 "D007020"
wdt:P492 "613679"
wdt:P493 "286.3"
"776.3"
wdt:P494 "D68.2"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0013361"
wdt:P6366 "2777260480"
wdt:P6532 Abnormal bleeding
menorrhagia
microhematuria
hemarthrosis
nosebleed
postpartum hemorrhage
cephalohematoma
intracranial hemorrhage
anemia
wdt:P665 "H01254"
wdt:P672 "C15.378.100.100.550"
"C15.378.100.141.550"
"C15.378.463.550"
"C16.320.099.550"
wdt:P699 "DOID:2235"
wdt:P780 bleeding
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