About: Sakati–Nyhan–Tisdale syndrome

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An Entity of Type : yago:WikicatGeneticDisordersWithOMIMButNoGene, within Data Space : wasabi.inria.fr associated with source document(s)

Sakati–Nyhan–Tisdale syndrome, is a rare genetic disorder that has been associated with abnormalities in the bones of the legs, congenital heart defects and craniofacial defects. The syndrome belongs to a group of rare genetic disorders known as acrocephalopolysyndactyly or ACPS, for short.

Attributes	Values
type	Thing disease yago:Abstraction100002137 yago:Attribute100024264 yago:Cognition100023271 yago:Condition113920835 yago:Content105809192 yago:Idea105833840 yago:PsychologicalFeature100023100 yago:State100024720 disease yago:WikicatCardiogeneticDisorders yago:Concept105835747 yago:Disease114070360 yago:Disorder114052403 yago:IllHealth114052046 yago:Illness114061805 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:Complex105870365 yago:GeneticDisease114151139 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatGeneticDisorders yago:WikicatSyndromes yago:WikicatGeneticDisordersWithOMIMButNoGene
label	Sakati–Nyhan–Tisdale syndrome Síndrome de Sakati-Nyhan-Tisdale متلازمة سقطي-نيهان-تيسديل
comment	متلازمة سقطي-نيهان-تيسديل (بالإنجليزية: Sakati–Nyhan–Tisdale syndrome)‏ أو تسنم الرأس وارتفاق الأصابع العنشي النوع الثالث (بالإنجليزية: acrocephalopolysyndactyly type III)‏ هي مرض وراثي نادر تظهر معه أعراض تشوهات في عظام الساقين ومرض قلبي خلقي وخلل .تنتمي المتلازمة إلى مجموعة من الاضطرابات الوراثية النادرة التي تعرف باسم تسنم الرأس وارتفاق الأصابع العنشي. El síndrome de Sakati-Nyan-Tisdale, también llamado acrocefalopolisindactilia tipo III, es una rara enfermedad de origen genético que pertenece al grupo de las acrocefalopolisindactilias o ACPS en abreviatura. Se caracteriza porque los niños afectados presentan anomalías en el desarrollo del cráneo (craneosinostosis), los huesos de las piernas, alteraciones cardiacas (cardiopatía congénita) y polidactilia. Fue descrita por primera vez en el año 1971 por los pediatras Nadia Aeni Sakati, William Leo Nyhan y W.K. Tisdale en la Universidad de California. Sakati–Nyhan–Tisdale syndrome, is a rare genetic disorder that has been associated with abnormalities in the bones of the legs, congenital heart defects and craniofacial defects. The syndrome belongs to a group of rare genetic disorders known as acrocephalopolysyndactyly or ACPS, for short.
sameAs	Sakati–Nyhan–Tisdale syndrome Sakati–Nyhan–Tisdale syndrome Sakati–Nyhan–Tisdale syndrome Sakati–Nyhan–Tisdale syndrome Sakati–Nyhan–Tisdale syndrome Sakati–Nyhan–Tisdale syndrome
name	Sakati–Nyhan–Tisdale syndrome
name	Sakati–Nyhan–Tisdale syndrome
topic	dbr:Carpenter_syndrome dbr:William_Nyhan dbr:Acrocephalosyndactyly dbr:List_of_modern_Arab_scientists_and_engineers dbr:Nyhan List of syndromes dbr:Nadia_Awni_Sakati dbr:Sakati-Nyhan-Tisdale_syndrome dbr:Sakati_syndrome wikipedia-en:Sakati–Nyhan–Tisdale_syndrome dbr:Sakati–Nyhan–Tisdale_syndrome#this
depiction
described by	https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Idea105833840 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Illness114061805 proxy:entity/http/dbpedia.org/class/yago/Idea105833840 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/resource/Disorder https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/resource/Template:Cn proxy:entity/http/dbpedia.org/resource/Genetic_disorder https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/resource/Category:Syndromes https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Syndrome105870790 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/PathologicalState114051917 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Disease114070360 proxy:entity/http/dbpedia.org/class/yago/Concept105835747 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Content105809192 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Condition113920835 proxy:entity/http/dbpedia.org/class/yago/Condition113920835 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/IllHealth114052046 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/class/yago/Disorder114052403 https://covidontheweb.inria.fr:4443/about/id/entity/http/dbpedia.org/resource/Syndactyly
subject	Genetic disorders with OMIM but no gene Cardiogenetic disorders Syndromes Congenital heart defects
Wikipage page ID	8600203(xsd:integer)
Wikipage revision ID	1052872146(xsd:integer)
Link from a Wikipage to another Wikipage	Craniosynostosis Joint Bone dbr:Apert_syndrome genetic disease Cyanosis Craniofacial United States Syria dbr:University_of_California,_San_Diego Congenital heart defect Genetic disorders with OMIM but no gene Cardiogenetic disorders syndactyly dbr:Acrocephalopolysyndactyly Syndromes Congenital heart defects dbr:Human_skull dbr:Genetic_mutation dbr:Crutches dbr:Nadia_Awni_Sakati dbr:William_Leo_Nyhan
is primary topic of	wikipedia-en:Sakati–Nyhan–Tisdale_syndrome
wasDerivedFrom	wikipedia-en:Sakati–Nyhan–Tisdale_syndrome?oldid=1052872146&ns=0
http://purl.org/li...ics/gold/hypernym	Disorder

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