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- Pierre_Robin_syndrome abstract "Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin sequence, Pierre Robin anomaly or Pierre Robin anomalad), is a congenital condition of facial abnormalities in humans. PRS is a sequence, i.e. a chain of certain developmental malformations, one entailing the next. The 3 main features are cleft palate, micrognathia (a small jaw) and glossoptosis (airway obstruction caused by backwards displacement of the tongue base). A genetic cause to PRS was recently identified. Pierre Robin sequence may be caused by genetic anomalies at chromosomes 2, 11, or 17.[citation needed]".
- Pierre_Robin_syndrome diseasesdb "29413".
- Pierre_Robin_syndrome emedicineSubject "ped".
- Pierre_Robin_syndrome emedicineTopic "2680".
- Pierre_Robin_syndrome icd10 "Q87.0".
- Pierre_Robin_syndrome icd9 "756.0".
- Pierre_Robin_syndrome medlineplus "001607".
- Pierre_Robin_syndrome meshId "D010855".
- Pierre_Robin_syndrome omim "261800".
- Pierre_Robin_syndrome wikiPageExternalLink ?aModele=afficheN&cpsidt=18787770.
- Pierre_Robin_syndrome wikiPageExternalLink mainpageS1894P0.html.
- Pierre_Robin_syndrome wikiPageExternalLink www.pierrerobin.com.
- Pierre_Robin_syndrome wikiPageExternalLink www.pierrerobin.org.
- Pierre_Robin_syndrome wikiPageExternalLink http://www.seattlechildrens.org/medical-conditions/chromosomal-genetic-conditions/pierre/#.
- Pierre_Robin_syndrome wikiPageExternalLink www.tremplin-spr.org.
- Pierre_Robin_syndrome wikiPageID "6013305".
- Pierre_Robin_syndrome wikiPageRevisionID "597609123".
- Pierre_Robin_syndrome diseasesdb "29413".
- Pierre_Robin_syndrome emedicinesubj "ped".
- Pierre_Robin_syndrome emedicinetopic "2680".
- Pierre_Robin_syndrome hasPhotoCollection Pierre_Robin_syndrome.
- Pierre_Robin_syndrome icd "756".
- Pierre_Robin_syndrome icd "Q87.0".
- Pierre_Robin_syndrome medlineplus "1607".
- Pierre_Robin_syndrome meshid "D010855".
- Pierre_Robin_syndrome name "Pierre Robin Sequence".
- Pierre_Robin_syndrome omim "261800".
- Pierre_Robin_syndrome wordnet_type synset-disease-noun-1.
- Pierre_Robin_syndrome subject Category:Congenital_disorders_of_musculoskeletal_system.
- Pierre_Robin_syndrome subject Category:Syndromes.
- Pierre_Robin_syndrome type Abnormality114501726.
- Pierre_Robin_syndrome type Abstraction100002137.
- Pierre_Robin_syndrome type Anomaly114505821.
- Pierre_Robin_syndrome type Attribute100024264.
- Pierre_Robin_syndrome type BirthDefect114465048.
- Pierre_Robin_syndrome type Cognition100023271.
- Pierre_Robin_syndrome type Complex105870365.
- Pierre_Robin_syndrome type Concept105835747.
- Pierre_Robin_syndrome type Condition113920835.
- Pierre_Robin_syndrome type CongenitalDisordersOfMusculoskeletalSystem.
- Pierre_Robin_syndrome type Content105809192.
- Pierre_Robin_syndrome type Defect114464005.
- Pierre_Robin_syndrome type Idea105833840.
- Pierre_Robin_syndrome type Imperfection114462666.
- Pierre_Robin_syndrome type PhysicalCondition114034177.
- Pierre_Robin_syndrome type PsychologicalFeature100023100.
- Pierre_Robin_syndrome type State100024720.
- Pierre_Robin_syndrome type Syndrome105870790.
- Pierre_Robin_syndrome type Syndromes.
- Pierre_Robin_syndrome type Whole105869584.
- Pierre_Robin_syndrome type Disease.
- Pierre_Robin_syndrome type AilmentCondition.
- Pierre_Robin_syndrome type Situation.
- Pierre_Robin_syndrome comment "Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation, Pierre Robin sequence, Pierre Robin anomaly or Pierre Robin anomalad), is a congenital condition of facial abnormalities in humans. PRS is a sequence, i.e. a chain of certain developmental malformations, one entailing the next. The 3 main features are cleft palate, micrognathia (a small jaw) and glossoptosis (airway obstruction caused by backwards displacement of the tongue base).".
- Pierre_Robin_syndrome label "Pierre Robin syndrome".
- Pierre_Robin_syndrome label "Pierre-Robin-Sequenz".
- Pierre_Robin_syndrome label "Sindrome di Pierre Robin".
- Pierre_Robin_syndrome label "Syndrome de Pierre Robin".
- Pierre_Robin_syndrome label "Syndroom van Pierre Robin".
- Pierre_Robin_syndrome label "Síndrome de Pierre Robin".
- Pierre_Robin_syndrome label "Síndrome de Pierre Robin".
- Pierre_Robin_syndrome label "Zespół Pierre'a Robina".
- Pierre_Robin_syndrome label "Синдром Робена".
- Pierre_Robin_syndrome sameAs Pierre-Robin-Sequenz.
- Pierre_Robin_syndrome sameAs Síndrome_de_Pierre_Robin.
- Pierre_Robin_syndrome sameAs Syndrome_de_Pierre_Robin.
- Pierre_Robin_syndrome sameAs Sindrome_di_Pierre_Robin.
- Pierre_Robin_syndrome sameAs Syndroom_van_Pierre_Robin.
- Pierre_Robin_syndrome sameAs Zespół_Pierre'a_Robina.
- Pierre_Robin_syndrome sameAs Síndrome_de_Pierre_Robin.
- Pierre_Robin_syndrome sameAs m.0fklh7.
- Pierre_Robin_syndrome sameAs Q1756040.
- Pierre_Robin_syndrome sameAs Q1756040.
- Pierre_Robin_syndrome sameAs Pierre_Robin_syndrome.
- Pierre_Robin_syndrome wasDerivedFrom Pierre_Robin_syndrome?oldid=597609123.
- Pierre_Robin_syndrome isPrimaryTopicOf Pierre_Robin_syndrome.
- Pierre_Robin_syndrome name "Pierre Robin Sequence".