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- Congenital_afibrinogenemia abstract "Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation.Fibrinogen is also known as Factor I. Its lack is inherited in an autosomic recessive way. It can express itself with excessive bleeding since birth (bleeding from umbilical cord, easy bruising, bleeding after circumcision)".
- Congenital_afibrinogenemia diseasesdb "307".
- Congenital_afibrinogenemia emedicineSubject "ped".
- Congenital_afibrinogenemia emedicineTopic "3042".
- Congenital_afibrinogenemia icd10 "D68.2".
- Congenital_afibrinogenemia icd9 "286.3".
- Congenital_afibrinogenemia medlineplus "001313".
- Congenital_afibrinogenemia meshId "D000347".
- Congenital_afibrinogenemia omim "202400".
- Congenital_afibrinogenemia wikiPageID "3250029".
- Congenital_afibrinogenemia wikiPageRevisionID "592702701".
- Congenital_afibrinogenemia diseasesdb "307".
- Congenital_afibrinogenemia emedicinesubj "ped".
- Congenital_afibrinogenemia emedicinetopic "3042".
- Congenital_afibrinogenemia hasPhotoCollection Congenital_afibrinogenemia.
- Congenital_afibrinogenemia icd "286.3".
- Congenital_afibrinogenemia icd "D68.2".
- Congenital_afibrinogenemia medlineplus "1313".
- Congenital_afibrinogenemia meshid "D000347".
- Congenital_afibrinogenemia name "Congenital afibrinogenemia".
- Congenital_afibrinogenemia omim "202400".
- Congenital_afibrinogenemia wordnet_type synset-disease-noun-1.
- Congenital_afibrinogenemia subject Category:Coagulopathies.
- Congenital_afibrinogenemia subject Category:Congenital_disorders.
- Congenital_afibrinogenemia type Disease.
- Congenital_afibrinogenemia type AilmentCondition.
- Congenital_afibrinogenemia type Situation.
- Congenital_afibrinogenemia comment "Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation.Fibrinogen is also known as Factor I. Its lack is inherited in an autosomic recessive way. It can express itself with excessive bleeding since birth (bleeding from umbilical cord, easy bruising, bleeding after circumcision)".
- Congenital_afibrinogenemia label "Afibrinogenemia".
- Congenital_afibrinogenemia label "Congenital afibrinogenemia".
- Congenital_afibrinogenemia sameAs Afibrinogenemia.
- Congenital_afibrinogenemia sameAs m.0917gf.
- Congenital_afibrinogenemia sameAs Q5160407.
- Congenital_afibrinogenemia sameAs Q5160407.
- Congenital_afibrinogenemia sameAs 46.
- Congenital_afibrinogenemia wasDerivedFrom Congenital_afibrinogenemia?oldid=592702701.
- Congenital_afibrinogenemia isPrimaryTopicOf Congenital_afibrinogenemia.
- Congenital_afibrinogenemia name "Congenital afibrinogenemia".