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- Jacobsen_syndrome abstract "Jacobsen Syndrome, also known as 11q deletion disorder, is a rare congenital disorder resulting from deletion of a terminal region of chromosome 11 that includes band 11q24.1. It can cause intellectual disabilities, a distinctive facial appearance, and a variety of physical problems including heart defects and a bleeding disorder. The syndrome was first identified by Danish physician Petra Jacobsen, and is believed to occur in approximately 1 out of every 100,000 births.".
- Jacobsen_syndrome diseasesdb "31957".
- Jacobsen_syndrome icd10 "Q93.5".
- Jacobsen_syndrome icd9 "758.3".
- Jacobsen_syndrome omim "147791".
- Jacobsen_syndrome wikiPageExternalLink www.11qusa.org.
- Jacobsen_syndrome wikiPageExternalLink www.chromosome11.eu.
- Jacobsen_syndrome wikiPageExternalLink clinodactyly.html.
- Jacobsen_syndrome wikiPageID "1840468".
- Jacobsen_syndrome wikiPageRevisionID "605686471".
- Jacobsen_syndrome caption "Girl with Jacobsen syndrome".
- Jacobsen_syndrome diseasesdb "31957".
- Jacobsen_syndrome hasPhotoCollection Jacobsen_syndrome.
- Jacobsen_syndrome icd "758.3".
- Jacobsen_syndrome icd "Q93.5".
- Jacobsen_syndrome name "Jacobsen syndrome".
- Jacobsen_syndrome omim "147791".
- Jacobsen_syndrome wordnet_type synset-disease-noun-1.
- Jacobsen_syndrome subject Category:Autosomal_monosomies_and_deletions.
- Jacobsen_syndrome type Aberrance114503665.
- Jacobsen_syndrome type Abnormality114501726.
- Jacobsen_syndrome type Abstraction100002137.
- Jacobsen_syndrome type Attribute100024264.
- Jacobsen_syndrome type AutosomalMonosomiesAndDeletions.
- Jacobsen_syndrome type ChromosomalAberration114504103.
- Jacobsen_syndrome type Condition113920835.
- Jacobsen_syndrome type Disease114070360.
- Jacobsen_syndrome type IllHealth114052046.
- Jacobsen_syndrome type Illness114061805.
- Jacobsen_syndrome type Monosomy114504405.
- Jacobsen_syndrome type PathologicalState114051917.
- Jacobsen_syndrome type PhysicalCondition114034177.
- Jacobsen_syndrome type State100024720.
- Jacobsen_syndrome type Disease.
- Jacobsen_syndrome type AilmentCondition.
- Jacobsen_syndrome type Situation.
- Jacobsen_syndrome comment "Jacobsen Syndrome, also known as 11q deletion disorder, is a rare congenital disorder resulting from deletion of a terminal region of chromosome 11 that includes band 11q24.1. It can cause intellectual disabilities, a distinctive facial appearance, and a variety of physical problems including heart defects and a bleeding disorder. The syndrome was first identified by Danish physician Petra Jacobsen, and is believed to occur in approximately 1 out of every 100,000 births.".
- Jacobsen_syndrome label "Jacobsen syndrome".
- Jacobsen_syndrome label "Jacobsen-Syndrom".
- Jacobsen_syndrome label "Sindrome di Jacobsen".
- Jacobsen_syndrome label "Syndrome de Jacobsen".
- Jacobsen_syndrome label "Syndroom van Jacobsen".
- Jacobsen_syndrome label "Síndrome de Jacobsen".
- Jacobsen_syndrome label "Zespół Jacobsena".
- Jacobsen_syndrome sameAs Jacobsen-Syndrom.
- Jacobsen_syndrome sameAs Síndrome_de_Jacobsen.
- Jacobsen_syndrome sameAs Syndrome_de_Jacobsen.
- Jacobsen_syndrome sameAs Sindrome_di_Jacobsen.
- Jacobsen_syndrome sameAs 제이콥슨_증후군.
- Jacobsen_syndrome sameAs Syndroom_van_Jacobsen.
- Jacobsen_syndrome sameAs Zespół_Jacobsena.
- Jacobsen_syndrome sameAs m.06024x.
- Jacobsen_syndrome sameAs Q1677755.
- Jacobsen_syndrome sameAs Q1677755.
- Jacobsen_syndrome sameAs Jacobsen_syndrome.
- Jacobsen_syndrome wasDerivedFrom Jacobsen_syndrome?oldid=605686471.
- Jacobsen_syndrome isPrimaryTopicOf Jacobsen_syndrome.
- Jacobsen_syndrome name "Jacobsen syndrome".