Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Pfeiffer_syndrome> ?p ?o. }
Showing items 1 to 60 of
60
with 100 items per page.
- Pfeiffer_syndrome abstract "Pfeiffer syndrome is a rare genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. Pfeiffer syndrome also affects bones in the hands and feet. It is named after Rudolf Arthur Pfeiffer (b. 1931) who, in 1964, described a list of features that included a coronal synostosis, turribrachycephaly (high prominent forehead) and maxillary hypoplasia (eyes with a bulging appearance due to small underlying cheek bones). Pfeiffer syndrome affects about 1 in 100,000 births.".
- Pfeiffer_syndrome diseasesdb "32145".
- Pfeiffer_syndrome meshId "D000168".
- Pfeiffer_syndrome omim "101600".
- Pfeiffer_syndrome wikiPageExternalLink br.fcgi?book=gene&part=craniosynostosis.
- Pfeiffer_syndrome wikiPageID "3443689".
- Pfeiffer_syndrome wikiPageRevisionID "592772082".
- Pfeiffer_syndrome diseasesdb "32145".
- Pfeiffer_syndrome hasPhotoCollection Pfeiffer_syndrome.
- Pfeiffer_syndrome meshid "D000168".
- Pfeiffer_syndrome name "Pfeiffer syndrome".
- Pfeiffer_syndrome omim "101600".
- Pfeiffer_syndrome wordnet_type synset-disease-noun-1.
- Pfeiffer_syndrome subject Category:Cell_surface_receptor_deficiencies.
- Pfeiffer_syndrome subject Category:Genodermatoses.
- Pfeiffer_syndrome subject Category:Syndromes.
- Pfeiffer_syndrome type Abstraction100002137.
- Pfeiffer_syndrome type Attribute100024264.
- Pfeiffer_syndrome type CellSurfaceReceptorDeficiencies.
- Pfeiffer_syndrome type Cognition100023271.
- Pfeiffer_syndrome type Complex105870365.
- Pfeiffer_syndrome type Concept105835747.
- Pfeiffer_syndrome type Condition113920835.
- Pfeiffer_syndrome type Content105809192.
- Pfeiffer_syndrome type Disease114070360.
- Pfeiffer_syndrome type Idea105833840.
- Pfeiffer_syndrome type IllHealth114052046.
- Pfeiffer_syndrome type Illness114061805.
- Pfeiffer_syndrome type Lack114449405.
- Pfeiffer_syndrome type Need114449126.
- Pfeiffer_syndrome type PathologicalState114051917.
- Pfeiffer_syndrome type PhysicalCondition114034177.
- Pfeiffer_syndrome type PsychologicalFeature100023100.
- Pfeiffer_syndrome type State100024720.
- Pfeiffer_syndrome type Syndrome105870790.
- Pfeiffer_syndrome type Syndromes.
- Pfeiffer_syndrome type Whole105869584.
- Pfeiffer_syndrome type Disease.
- Pfeiffer_syndrome type AilmentCondition.
- Pfeiffer_syndrome type Situation.
- Pfeiffer_syndrome comment "Pfeiffer syndrome is a rare genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. Pfeiffer syndrome also affects bones in the hands and feet. It is named after Rudolf Arthur Pfeiffer (b.".
- Pfeiffer_syndrome label "Pfeiffer syndrome".
- Pfeiffer_syndrome label "Pfeiffer-Syndrom".
- Pfeiffer_syndrome label "Syndrome de Pfeiffer".
- Pfeiffer_syndrome label "Syndroom van Pfeiffer".
- Pfeiffer_syndrome label "Síndrome de Pfeiffer".
- Pfeiffer_syndrome label "Zespół Pfeiffera".
- Pfeiffer_syndrome sameAs Pfeiffer-Syndrom.
- Pfeiffer_syndrome sameAs Síndrome_de_Pfeiffer.
- Pfeiffer_syndrome sameAs Syndrome_de_Pfeiffer.
- Pfeiffer_syndrome sameAs Syndroom_van_Pfeiffer.
- Pfeiffer_syndrome sameAs Zespół_Pfeiffera.
- Pfeiffer_syndrome sameAs m.09cqjr.
- Pfeiffer_syndrome sameAs Q1286848.
- Pfeiffer_syndrome sameAs Q1286848.
- Pfeiffer_syndrome sameAs 918.
- Pfeiffer_syndrome sameAs Pfeiffer_syndrome.
- Pfeiffer_syndrome wasDerivedFrom Pfeiffer_syndrome?oldid=592772082.
- Pfeiffer_syndrome isPrimaryTopicOf Pfeiffer_syndrome.
- Pfeiffer_syndrome name "Pfeiffer syndrome".