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- Factor_XIII_deficiency abstract "Factor XIII deficiency may occur very rarely, and can cause a severe bleeding tendency. The incidence is 1 in a million to 1 in 5 million people. Most are due to mutations in the A subunit gene (located on chromosome 6p25-p24). This mutation is inherited in an autosomal recessive fashion.As Factor XIII is composed of two subunit protein A and B, for which the genes are located on different chromosomes, administration of recombinant A subunit improves clot stability and is becoming a therapeutic option for patients with this condition. This deficiency leads to defective cross-linking of fibrin and vulnerability to late re-bleeds when the primary hemostatic plug is overwhelmed. Bleeding tendencies similar to hemophiliacs develop such as hemarthroses and deep tissue bleeding.".
- Factor_XIII_deficiency diseasesdb "31412".
- Factor_XIII_deficiency emedicineSubject "ped".
- Factor_XIII_deficiency emedicineTopic "3040".
- Factor_XIII_deficiency icd10 "D68.2".
- Factor_XIII_deficiency icd9 "286.3".
- Factor_XIII_deficiency meshId "D005177".
- Factor_XIII_deficiency omim "134570".
- Factor_XIII_deficiency wikiPageID "4304755".
- Factor_XIII_deficiency wikiPageRevisionID "563067257".
- Factor_XIII_deficiency diseasesdb "31412".
- Factor_XIII_deficiency emedicinesubj "ped".
- Factor_XIII_deficiency emedicinetopic "3040".
- Factor_XIII_deficiency hasPhotoCollection Factor_XIII_deficiency.
- Factor_XIII_deficiency icd "286.3".
- Factor_XIII_deficiency icd "D68.2".
- Factor_XIII_deficiency meshid "D005177".
- Factor_XIII_deficiency name "Factor XIII deficiency".
- Factor_XIII_deficiency omim "134570".
- Factor_XIII_deficiency wordnet_type synset-disease-noun-1.
- Factor_XIII_deficiency subject Category:Coagulopathies.
- Factor_XIII_deficiency subject Category:Haemophilia.
- Factor_XIII_deficiency type Abstraction100002137.
- Factor_XIII_deficiency type Attribute100024264.
- Factor_XIII_deficiency type Condition113920835.
- Factor_XIII_deficiency type Disease114070360.
- Factor_XIII_deficiency type IllHealth114052046.
- Factor_XIII_deficiency type Illness114061805.
- Factor_XIII_deficiency type PathologicalState114051917.
- Factor_XIII_deficiency type PhysicalCondition114034177.
- Factor_XIII_deficiency type State100024720.
- Factor_XIII_deficiency type Disease.
- Factor_XIII_deficiency type AilmentCondition.
- Factor_XIII_deficiency type Situation.
- Factor_XIII_deficiency comment "Factor XIII deficiency may occur very rarely, and can cause a severe bleeding tendency. The incidence is 1 in a million to 1 in 5 million people. Most are due to mutations in the A subunit gene (located on chromosome 6p25-p24).".
- Factor_XIII_deficiency label "Factor XIII deficiency".
- Factor_XIII_deficiency label "Faktor-XIII-Mangel".
- Factor_XIII_deficiency sameAs Faktor-XIII-Mangel.
- Factor_XIII_deficiency sameAs m.02wvby0.
- Factor_XIII_deficiency sameAs Q1393725.
- Factor_XIII_deficiency sameAs Q1393725.
- Factor_XIII_deficiency sameAs 2367.
- Factor_XIII_deficiency sameAs 2368.
- Factor_XIII_deficiency sameAs 2369.
- Factor_XIII_deficiency sameAs Factor_XIII_deficiency.
- Factor_XIII_deficiency wasDerivedFrom Factor_XIII_deficiency?oldid=563067257.
- Factor_XIII_deficiency isPrimaryTopicOf Factor_XIII_deficiency.
- Factor_XIII_deficiency name "Factor XIII deficiency".