About: Fraser syndrome

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Fraser syndrome (also known as Meyer-Schwickerath's syndrome, Fraser-François syndrome, or Ullrich-Feichtiger syndrome) is an autosomal recessive congenital disorder, identified by several developmental anomalies. Fraser syndrome is named for the geneticist George R. Fraser, who first described the syndrome in 1962.

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rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Disease114070360 yago:Disorder114052403 yago:GeneticDisease114151139 yago:IllHealth114052046 yago:Illness114061805 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:WikicatGeneticDisorders disease yago:State100024720 umbel-rc:AilmentCondition
rdfs:label	فرسر سيندروم (ar) Fraser-Syndrom (de) Fraser syndrome (en) Zespół Frasera (pl) Синдром Фрейзера (ru)
rdfs:comment	Das Fraser-Syndrom ist eine äußerst seltene Mutation, die bislang bei etwa 150 Kindern beschrieben wurde. Die Besonderheit geht hauptsächlich mit körperlichen Fehlbildungen einher. Viele der betroffenen Kinder sterben während oder unmittelbar nach der Geburt, da meist Kehlkopf- und Nierenfehlbildungen vorhanden sind. (de) فرسر سيندروم (بالإنجليزية: Fraser syndrome)‏ هو عيب خلقي وراثي جسمي نادر، تم تسميته نسبة إلى عالم الوراثة الذي وصفه عام 1962. (ar) Fraser syndrome (also known as Meyer-Schwickerath's syndrome, Fraser-François syndrome, or Ullrich-Feichtiger syndrome) is an autosomal recessive congenital disorder, identified by several developmental anomalies. Fraser syndrome is named for the geneticist George R. Fraser, who first described the syndrome in 1962. (en) Zespół Frasera (zespół Meyera-Schwickeratha, zespół Fraser-François, zespół Ullricha-Feichtigera, ang. Fraser syndrome, Meyer-Schwickerath's syndrome, Fraser-François syndrome, Ullrich-Feichtiger syndrome) – zespół wad wrodzonych spowodowany mutacjami w genie lub , charakteryzujący się skrytooczem (cryptophthalmos) i skojarzonymi malformacjami innych układów narządów, zwłaszcza układu moczowego i oddechowego. Został opisany przez brytyjskiego genetyka George'a R. Frasera w 1962 roku. Dziedziczenie zespołu jest autosomalne recesywne. (pl) Синдром Фрейзера (синдром Мейер-Швикерата, синдром Фрейзера—Франсуа) — аутосомно-рецессивное врождённое заболевание. Синдром назван по имени медицинского генетика Джорджа Фрейзера. (ru)
foaf:name	Fraser syndrome (en)
name	Fraser syndrome (en)
foaf:depiction
dcterms:subject	Autosomal recessive disorders Rare syndromes Syndromes affecting the eye Syndromes with intellectual disability Syndromes affecting female reproductive system
Wikipage page ID	2670970 (xsd:integer)
Wikipage revision ID	1111782939 (xsd:integer)
Link from a Wikipage to another Wikipage	FREM2 Morphogenesis Renal Intersex Cryptorchidism Genitals Cryptophthalmos Autosomal recessive disorders Clitoromegaly Autosomal Micropenis Ear Glutamate receptor-interacting protein Rare syndromes Syndromes affecting the eye Syndromes with intellectual disability Larynx Syndactyly George R. Fraser Syndromes affecting female reproductive system Autopsy Human nose Recessive FRAS1 Congenital Congenital abnormality Oligohydramnios Microphthalmos Developmental delays Perinatal Malformation Clinical examination
sameAs	Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome Fraser syndrome
SNOMED CT	204102004 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:For dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Short_description
thumbnail	wiki-commons:Special:FilePath/Fraser_syndrome.gif?width=300
DiseasesDB	32241 (xsd:integer)
ICD	(en) Q87.0 (en)
OMIM	219000 (xsd:integer)
Orphanet	2052 (xsd:integer)

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