About: OSLAM syndrome

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OSLAM syndrome is a rare autosomal dominant hereditary disorder. Its name is an initialism of "osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome". OSLAM syndrome was recognised and described by Mulvilhill et al. as a syndrome that increases susceptibility to tumours and is characterised by an impaired regulation of bone and marrow development. Individuals with OSLAM syndrome have an elevated risk of bone cancer, limb abnormalities, and enlarged red blood cells.

Attributes	Values
rdf:type	Thing Disease yago:Abstraction100002137 yago:Attribute100024264 yago:Cancer114239918 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Disease114070360 yago:Growth114234074 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:Malignancy114237561 yago:MalignantTumor114239425 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatHereditaryCancers disease yago:State100024720 yago:Syndrome105870790 yago:Tumor114235200 yago:Whole105869584 yago:WikicatSyndromes
rdfs:label	متلازمة أوسلام (ar) OSLAM syndrome (en)
rdfs:comment	متلازمة أوسلام (بالإنجليزية: OSALM Syndrome)‏ هو سيادة وراثية مرضية تامة الاسم هو اختصار ل:سرطان عظمي، تشوهات خلقية للأطراف، كثرة كريات الدم الحمراء مع متلازمة نخاع الارومات الضخمة. وُجدت هذة المتلازمة ووُصفت من قبل Muluihill etal، وهذة المتلازمة تزيد نسبة حدوث الاورام وتتميز بنمو العظام الضعيف وتطوير النخاع. تعد متلازمة أوسلام مرضاً وراثياً ذات سيادة مرضية تامة. مصابي افراد متلازمة OSLAM لديهم مخاطر عالية للإصابة بسرطان العظام والأطراف الشاذة وتضخم خلايا الدم الحمراء. (ar) OSLAM syndrome is a rare autosomal dominant hereditary disorder. Its name is an initialism of "osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome". OSLAM syndrome was recognised and described by Mulvilhill et al. as a syndrome that increases susceptibility to tumours and is characterised by an impaired regulation of bone and marrow development. Individuals with OSLAM syndrome have an elevated risk of bone cancer, limb abnormalities, and enlarged red blood cells. (en)
foaf:depiction
dcterms:subject	Osseous and chondromatous neoplasia Sarcoma Hereditary cancers Syndromes
Wikipage page ID	34177892 (xsd:integer)
Wikipage revision ID	1050515105 (xsd:integer)
Link from a Wikipage to another Wikipage	Hereditary disorder Clinodactyly Macrocytosis Autosomal dominant Osseous and chondromatous neoplasia Sarcoma Osteosarcoma Hereditary cancers Syndromes Radioulnar synostosis Li-Fraumeni syndrome
sameAs	OSLAM syndrome OSLAM syndrome OSLAM syndrome OSLAM syndrome OSLAM syndrome OSLAM syndrome
dbp:wikiPageUsesTemplate	dbt:Genetic-disorder-stub dbt:Cn dbt:Empty_section dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:PAGENAME dbt:Reflist dbt:Abbreviation
thumbnail	wiki-commons:Special:FilePath/Autosomal_dominant_-_en.svg?width=300
deaths	idk (en)
ICD	41.9 (nicaraguanCórdoba)
OMIM	165660 (xsd:integer)
Orphanet	2760 (xsd:integer)
caption	OSLAM syndrome is inherited in an autosomal dominant manner (en)
synonyms	Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome (en)
has abstract	متلازمة أوسلام (بالإنجليزية: OSALM Syndrome)‏ هو سيادة وراثية مرضية تامة الاسم هو اختصار ل:سرطان عظمي، تشوهات خلقية للأطراف، كثرة كريات الدم الحمراء مع متلازمة نخاع الارومات الضخمة. وُجدت هذة المتلازمة ووُصفت من قبل Muluihill etal، وهذة المتلازمة تزيد نسبة حدوث الاورام وتتميز بنمو العظام الضعيف وتطوير النخاع. تعد متلازمة أوسلام مرضاً وراثياً ذات سيادة مرضية تامة. مصابي افراد متلازمة OSLAM لديهم مخاطر عالية للإصابة بسرطان العظام والأطراف الشاذة وتضخم خلايا الدم الحمراء. (ar) OSLAM syndrome is a rare autosomal dominant hereditary disorder. Its name is an initialism of "osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome". OSLAM syndrome was recognised and described by Mulvilhill et al. as a syndrome that increases susceptibility to tumours and is characterised by an impaired regulation of bone and marrow development. Individuals with OSLAM syndrome have an elevated risk of bone cancer, limb abnormalities, and enlarged red blood cells. (en)
MeSH	537138.0 (nicaraguanCórdoba)
gold:hypernym	Disorder
prov:wasDerivedFrom	wikipedia-en:OSLAM_syndrome?oldid=1050515105&ns=0
page length (characters) of wiki page	2674 (xsd:nonNegativeInteger)
ICD10	C41.9
OMIM id	165660 (xsd:integer)
ORPHA	2760
foaf:isPrimaryTopicOf	wikipedia-en:OSLAM_syndrome
is Link from a Wikipage to another Wikipage of	List of diseases (O) Clinodactyly Li–Fraumeni syndrome List of syndromes Oslam syndrome Osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome
is Wikipage redirect of	Oslam syndrome Osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow syndrome
is foaf:primaryTopic of	wikipedia-en:OSLAM_syndrome

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