About: Chromosome 5q deletion syndrome

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Chromosome 5q deletion syndrome is an acquired, hematological disorder characterized by loss of part of the long arm (q arm, band 5q33.1) of human chromosome 5 in bone marrow myelocyte cells. This chromosome abnormality is most commonly associated with the myelodysplastic syndrome. It should not be confused with "partial trisomy 5q", though both conditions have been observed in the same family.This should not be confused with the germ line cri du chat (5p deletion) syndrome which is a deletion of the short arm of the 5th chromosome.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalMonosomiesAndDeletions yago:Aberrance114503665 yago:Abnormality114501726 yago:Abstraction100002137 yago:Attribute100024264 yago:ChromosomalAberration114504103 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Disease114070360 yago:GeneticDisease114151139 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:Monosomy114504405 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatGeneticDisorders disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes umbel-rc:AilmentCondition
rdfs:label	Chromosome 5q deletion syndrome (en) 5q-minus-Syndrom (de) Síndrome del 5q (es) Syndrome 5q- (fr) 5q-症候群 (ja) 5號染色體長臂缺失症候群 (zh)
rdfs:comment	Chromosome 5q deletion syndrome is an acquired, hematological disorder characterized by loss of part of the long arm (q arm, band 5q33.1) of human chromosome 5 in bone marrow myelocyte cells. This chromosome abnormality is most commonly associated with the myelodysplastic syndrome. It should not be confused with "partial trisomy 5q", though both conditions have been observed in the same family.This should not be confused with the germ line cri du chat (5p deletion) syndrome which is a deletion of the short arm of the 5th chromosome. (en) 5q-症候群(ファイブ・キュー・マイナスしょうこうぐん英名：5q-syndrome)とは骨髄異形成症候群(MDS）の一種で造血細胞の5番染色体の長椀(5q)に欠失が生じたことが原因で発症し、大球性貧血を特徴とする骨髄異形成症候群(MDS）のなかでは進行のゆっくりとした比較的予後の良い血液疾患である。ただし、5番染色体の長椀の一部だけでなく一本を丸々失ったもの（モノソミー5、monosomy5）や5q以外にも異常を伴ったものは一般に極めて悪性度が高いMDSであり、本稿で述べる5q-症候群とは異なる。 (ja) 5號染色體長臂缺失症候群（Chromosome 5q deletion syndrome、5q症候群、5號長臂(monosomy)、5號染色體長臂缺失綜合症）是一種血液疾病，特徵是人類5號染色體「長臂」（q arm, band 5q31.1）的一部分缺失。這種染色體異常最常見伴隨著骨髓增生异常综合征（MDS）而產生。它不與“5號長臂部分染色體三倍體症（partial trisomy 5q）”等同，雖然這兩種病症的產生都在同一個系列裡可以觀察的到。此種症狀不能和猫叫综合症混為一談，因猫叫综合症是一種缺失第5號染色體「短臂」（p arm/petit）的症候群。 (zh) Das 5q-minus-Syndrom gehört zur Gruppe der Myelodysplastischen Syndrome (MDS). Es ist zytogenetisch gekennzeichnet durch den Verlust eines Teils des Chromosoms 5 (langer Arm von Chromosom 5 = 5q) und hat daher seinen Namen erhalten. (de) El Síndrome del 5q es una enfermedad muy poco frecuente causada por la pérdida (deleción) de una parte del brazo largo del cromosoma 5 (en terminología médica a dicho brazo se le denomina 5q). Afecta fundamentalmente a las células de la serie ósea, provocando anemia refractaria al tratamiento y síndromes mielodisplásicos que pueden derivar hacia la leucemia aguda. El estudio de la serie ósea muestra cambios característicos en los megacariocitos: aumenta su número y se vuelven más pequeños y mononucleares. A veces puede acompañarse de hiperplasia eritroide. (es) Le syndrome 5q- est une forme particulière de myélodysplasie. Syndrome 5q- Microphotographie de moelle osseuse montrant les mégacaryocytes mononucléaires anormaux caractéristiques du syndrome 5q-. Mise en garde médicale Elle ne doit pas être confondue avec la maladie du cri du chat, qui est causée par une délétion du bras court du chromosome 5. (fr)
name	Chromosome 5q deletion syndrome (en)
foaf:depiction
dcterms:subject	Autosomal monosomies and deletions Myeloid neoplasia Rare syndromes Syndromes affecting blood
Wikipage page ID	1300703 (xsd:integer)
Wikipage revision ID	1094371754 (xsd:integer)
Link from a Wikipage to another Wikipage	Pure red cell aplasia Megakaryocyte RPS14 Trisomy CDC25C Dysplasia EGR1 dbr:P53 Q arm Megakaryocytes dbr:Osteonectin Thrombocytosis Gene Myelodysplastic syndrome Monosomy Autosomal monosomies and deletions Anemia Lenalidomide Tumor suppressor gene MiR-146 Lobation Mir-145 FDA Cell nucleus Myeloid neoplasia Chromosome 5 Haploinsufficiency Rare syndromes Acute myelogenous leukemia Hyperplasia Syndromes affecting blood Pathogenesis Bone marrow Macrocytic anemia Catenin (cadherin-associated protein), alpha 1 Myelocyte Cri du chat Germ line
sameAs	Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome Chromosome 5q deletion syndrome
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Cn dbt:Medical_resources

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