About: Greig cephalopolysyndactyly syndrome

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About: Greig cephalopolysyndactyly syndrome Goto Sponge NotDistinct Permalink

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Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. The features of this syndrome are highly variable, ranging from very mild to severe. People with this condition typically have one or more extra fingers or toes (polydactyly) or an abnormally wide thumb or big toe (hallux).

Attributes	Values
rdf:type	Thing Fuchs' dystrophy yago:WikicatAutosomalDominantDisorders yago:WikicatCongenitalDisordersOfMusculoskeletalSystem yago:WikicatTranscriptionFactorDeficiencies yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:AutosomalDominantDisease114162025 yago:BirthDefect114465048 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Defect114464005 yago:Disease114070360 yago:GeneticDisease114151139 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:Lack114449405 yago:Need114449126 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatGeneticDisorders disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes umbel-rc:AilmentCondition
rdfs:label	متلازمة غريغ سيفالو بولي سايندكتلي (ar) Greig-Syndrom (de) Greig cephalopolysyndactyly syndrome (en) Syndrome de Greig (fr) Sindrome di Greig (it) Zespół Greiga (pl)
rdfs:comment	متلازمة غريغ سيفالو بولي سايندكتلي هي اضطراب يؤثر على نمو الأطراف والرأس والوجه. تتنوع سمات هذه المتلازمة بدرجة كبيرة، وتتراوح من خفيفة جدًا إلى شديدة. عادةً ما يكون لدى الأشخاص الذين يعانون من هذه الحالة إصبع أو أصابع إضافية واحدة أو أكثر (تعدد أصابع) أو إبهام عريض بشكل غير طبيعي أو إصبع كبير (إبهام القدم). (ar) Greig cephalopolysyndactyly syndrome is a disorder that affects development of the limbs, head, and face. The features of this syndrome are highly variable, ranging from very mild to severe. People with this condition typically have one or more extra fingers or toes (polydactyly) or an abnormally wide thumb or big toe (hallux). (en) La sindrome di Greig o cefalopolisindattilia di Greig è una malattia genetica rara caratterizzata da dismorfismo cranio-facciale, polidattilia e sindattilia. (it) Zespół Greiga (zespół Greiga I, cefalopolisyndaktylia Greiga, ang. Greig cephalopolysyndactyly syndrome, CPSG) – rzadki zespół wad wrodzonych, na który składają się wysokie i szerokie czoło, hiperteloryzm oczny, syndaktylia dłoni i stóp z polidaktylią przedosiową. (pl) Das Greig-Syndrom ist eine angeborene Erkrankung mit einer charakteristischen Kombination von Schädel-Gesichtsdysmorphie und Polydaktylie (Vielgliedrigkeit der Finger). Synonyme sind: Greig-Zephalopolysyndaktylie-Syndrom; Zephalopolysyndaktylie; Hootnick-Holmes-Syndrom Nicht zu verwechseln ist der Familiäre Hypertelorismus Greig. (de) Le syndrome de Greig est une maladie génétique rare qui est caractérisée dans sa forme typique par l’association d’une polydactylie pré- ou postaxiale, d’un hypertélorisme orbitale et d’une macrocéphalie. Les anomalies du crane sont parfois subtiles. Les manifestations cliniques sont parfois plus limitées avec seulement une polydactylie préaxiale de type 4 et une polydactylie croisée : association d'une polydactylie préaxiale des pieds avec polydactylie postaxiale des mains avec syndactylie des troisième et quatrième doigts avec syndactylie des premier, second et troisième orteil. (fr)
foaf:name	Greig cephalopolysyndactyly syndrome (en)
name	Greig cephalopolysyndactyly syndrome (en)
foaf:depiction
dcterms:subject	Syndromes affecting head size Syndromes with dysmelia Rare syndromes Congenital disorders of musculoskeletal system Autosomal dominant disorders Transcription factor deficiencies
Wikipage page ID	4940778 (xsd:integer)
Wikipage revision ID	986080340 (xsd:integer)
Link from a Wikipage to another Wikipage	David Middleton Greig Gli3 Macrocephaly Autosomal dominant Acrocallosal syndrome Syndromes affecting head size Syndromes with dysmelia Rare syndromes Hallux Congenital disorders of musculoskeletal system Autosomal dominant disorders Transcription factor deficiencies Autosome Carpenter syndrome FRSE Polydactyly Gorlin Syndrome
Link from a Wikipage to an external page	https://www.ncbi.nlm.nih.gov/books/NBK1446/
sameAs	Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome Greig cephalopolysyndactyly syndrome
SNOMED CT	32985001 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Cn dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Redirect dbt:Reflist dbt:Congenital_malformations_and_deformations_of_musculoskeletal_system

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