About: McGillivray syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis (see this term) syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability

Property	Value
dbo:description	redek sindrom kraniosinostoze, za katerega so značilni skafocefalija, makrocefalija, huda retruzija zgornje čeljusti in blaga intelektualna oviranost (sl) Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis (see this term) syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability (en)
dbo:icd10	Q87.0
dbo:omim	609579 (xsd:integer)
dbo:orpha	168624
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dbo:wikiPageExternalLink	http://rarediseases.info.nih.gov/GARD/Disease.aspx%3FPageID=4&diseaseID=3426 https://www.ncbi.nlm.nih.gov/sites/ga%3Fdisorder=McGillivray%20syndrome https://docs.google.com/document/d/1Z4L2UUyAlfR6_E9pCgdWjdv0Y0kp8GeOJpRASUmn46Y/edit%23
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dbp:bot	medic (en)
dbp:caption	This condition is inherited via an autosomal dominant manner (en)
dbp:date	July 2025 (en)
dbp:field	cardiology (en)
dbp:icd	Q87.0 (en)
dbp:name	McGillivray syndrome (en)
dbp:omim	609579 (xsd:integer)
dbp:orphanet	168624 (xsd:integer)
dbp:synonyms	Familial scaphocephaly syndrome, McGillivray type, Scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome (en)
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gold:hypernym	dbr:Syndrome
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rdfs:label	McGillivray syndrome (en) متلازمة مكجيليفري (ar)
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prov:wasDerivedFrom	wikipedia-en:McGillivray_syndrome?oldid=1301340541&ns=0
foaf:depiction	wiki-commons:Special:FilePath/Autosomal_dominant_-_en.svg
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foaf:name	McGillivray syndrome (en)
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