Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Gray_platelet_syndrome> ?p ?o }
Showing triples 1 to 58 of
58
with 100 triples per page.
- Gray_platelet_syndrome abstract "Gray platelet syndrome (GPS), or platelet alpha-granule deficiency, is a rare congenital autosomal recessive bleeding disorder caused by a reduction or absence of alpha-granules in blood platelets, and the release of proteins normally contained in these granules into the marrow, causing myelofibrosis.GPS is primarily inherited in an autosomal recessive manner, and the gene that is mutated in GPS has recently been mapped to chromosome 3p and identified as NBEAL2. NBEAL2 encodes a protein containing a BEACH domain that is predicted to be involved in vesicular trafficking. It is expressed in platelets and megakaryocytes and is required for the development of platelet alpha-granules. NBEAL2 expression is also required for the development of thrombocytes in zebrafish.GPS is characterized by "thrombocytopenia, and abnormally large agranular platelets in peripheral blood smears." The defect in GPS is the failure of megakaryocytes to package secretory proteins into alpha-granules. Patients with the GPS are affected by mild to moderate bleeding tendencies.".
- Gray_platelet_syndrome icd10 "D69.1".
- Gray_platelet_syndrome omim "139090".
- Gray_platelet_syndrome wikiPageID "7337467".
- Gray_platelet_syndrome wikiPageLength "3816".
- Gray_platelet_syndrome wikiPageOutDegree "13".
- Gray_platelet_syndrome wikiPageRevisionID "678836124".
- Gray_platelet_syndrome wikiPageWikiLink Alpha-granules.
- Gray_platelet_syndrome wikiPageWikiLink Autosomal_recessive.
- Gray_platelet_syndrome wikiPageWikiLink Blood_platelet.
- Gray_platelet_syndrome wikiPageWikiLink Category:Autosomal_dominant_disorders.
- Gray_platelet_syndrome wikiPageWikiLink Category:Coagulopathies.
- Gray_platelet_syndrome wikiPageWikiLink Category:Genetic_disorders_with_OMIM_but_no_gene.
- Gray_platelet_syndrome wikiPageWikiLink Category:Rare_diseases.
- Gray_platelet_syndrome wikiPageWikiLink Category:Syndromes.
- Gray_platelet_syndrome wikiPageWikiLink Dominance_(genetics).
- Gray_platelet_syndrome wikiPageWikiLink Megakaryocyte.
- Gray_platelet_syndrome wikiPageWikiLink Myelofibrosis.
- Gray_platelet_syndrome wikiPageWikiLink Platelet.
- Gray_platelet_syndrome wikiPageWikiLink Platelet_alpha-granule.
- Gray_platelet_syndrome wikiPageWikiLink Protein.
- Gray_platelet_syndrome wikiPageWikiLink Pseudo_gray_platelet_syndrome.
- Gray_platelet_syndrome wikiPageWikiLink Thrombocytopenia.
- Gray_platelet_syndrome wikiPageWikiLinkText "Gray platelet syndrome".
- Gray_platelet_syndrome wikiPageWikiLinkText "gray platelet syndrome".
- Gray_platelet_syndrome diseasesdb "29160".
- Gray_platelet_syndrome hasPhotoCollection Gray_platelet_syndrome.
- Gray_platelet_syndrome icd "D69.1".
- Gray_platelet_syndrome medlineplus "582".
- Gray_platelet_syndrome name "Gray platelet syndrome".
- Gray_platelet_syndrome omim "139090".
- Gray_platelet_syndrome wikiPageUsesTemplate Template:Genetic-disorder-stub.
- Gray_platelet_syndrome wikiPageUsesTemplate Template:Hematology.
- Gray_platelet_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Gray_platelet_syndrome wikiPageUsesTemplate Template:RareDiseases.
- Gray_platelet_syndrome wikiPageUsesTemplate Template:Reflist.
- Gray_platelet_syndrome subject Category:Autosomal_dominant_disorders.
- Gray_platelet_syndrome subject Category:Coagulopathies.
- Gray_platelet_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Gray_platelet_syndrome subject Category:Rare_diseases.
- Gray_platelet_syndrome subject Category:Syndromes.
- Gray_platelet_syndrome hypernym Disorder.
- Gray_platelet_syndrome type Disease.
- Gray_platelet_syndrome type Disorder.
- Gray_platelet_syndrome type Syndrome.
- Gray_platelet_syndrome type Thing.
- Gray_platelet_syndrome type Q12136.
- Gray_platelet_syndrome comment "Gray platelet syndrome (GPS), or platelet alpha-granule deficiency, is a rare congenital autosomal recessive bleeding disorder caused by a reduction or absence of alpha-granules in blood platelets, and the release of proteins normally contained in these granules into the marrow, causing myelofibrosis.GPS is primarily inherited in an autosomal recessive manner, and the gene that is mutated in GPS has recently been mapped to chromosome 3p and identified as NBEAL2.".
- Gray_platelet_syndrome label "Gray platelet syndrome".
- Gray_platelet_syndrome sameAs Syndrome_des_plaquettes_grises.
- Gray_platelet_syndrome sameAs Sindrome_delle_piastrine_grigie.
- Gray_platelet_syndrome sameAs Zespół_szarych_płytek.
- Gray_platelet_syndrome sameAs m.01xn0ps.
- Gray_platelet_syndrome sameAs Q5598273.
- Gray_platelet_syndrome sameAs Q5598273.
- Gray_platelet_syndrome wasDerivedFrom Gray_platelet_syndrome?oldid=678836124.
- Gray_platelet_syndrome isPrimaryTopicOf Gray_platelet_syndrome.
- Gray_platelet_syndrome name "Gray platelet syndrome".