Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Watson_syndrome> ?p ?o }
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- Watson_syndrome abstract "Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.".
- Watson_syndrome icd10 "Q87.1".
- Watson_syndrome meshId "D009456".
- Watson_syndrome omim "193520".
- Watson_syndrome wikiPageID "24167376".
- Watson_syndrome wikiPageLength "1578".
- Watson_syndrome wikiPageOutDegree "13".
- Watson_syndrome wikiPageRevisionID "679115166".
- Watson_syndrome wikiPageWikiLink Allele.
- Watson_syndrome wikiPageWikiLink Category:Genodermatoses.
- Watson_syndrome wikiPageWikiLink Genetic_disorder.
- Watson_syndrome wikiPageWikiLink Lisch_nodule.
- Watson_syndrome wikiPageWikiLink List_of_cutaneous_conditions.
- Watson_syndrome wikiPageWikiLink Macrocephaly.
- Watson_syndrome wikiPageWikiLink Neurofibroma.
- Watson_syndrome wikiPageWikiLink Neurofibromatosis_type_I.
- Watson_syndrome wikiPageWikiLink Neurofibromin_1.
- Watson_syndrome wikiPageWikiLink Ocular_iris.
- Watson_syndrome wikiPageWikiLink Pulmonary_valvular_stenosis.
- Watson_syndrome wikiPageWikiLink Short_stature.
- Watson_syndrome wikiPageWikiLink Westerhof_syndrome.
- Watson_syndrome wikiPageWikiLinkText "Watson syndrome".
- Watson_syndrome diseasesdb "32244".
- Watson_syndrome icd "Q87.1".
- Watson_syndrome meshid "D009456".
- Watson_syndrome name "Watson syndrome".
- Watson_syndrome omim "193520".
- Watson_syndrome wikiPageUsesTemplate Template:Deficiencies_of_intracellular_signaling_peptides_and_proteins.
- Watson_syndrome wikiPageUsesTemplate Template:Genodermatoses-stub.
- Watson_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Watson_syndrome wikiPageUsesTemplate Template:Phakomatoses.
- Watson_syndrome wikiPageUsesTemplate Template:Reflist.
- Watson_syndrome subject Category:Genodermatoses.
- Watson_syndrome hypernym Condition.
- Watson_syndrome type Disease.
- Watson_syndrome type Disorder.
- Watson_syndrome type Thing.
- Watson_syndrome type Q12136.
- Watson_syndrome comment "Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.".
- Watson_syndrome label "Watson syndrome".
- Watson_syndrome sameAs Q1112752.
- Watson_syndrome sameAs Watsonin_oireyhtymä.
- Watson_syndrome sameAs Syndrome_de_Watson.
- Watson_syndrome sameAs m.07k4wpr.
- Watson_syndrome sameAs Q1112752.
- Watson_syndrome sameAs 沃森综合征.
- Watson_syndrome wasDerivedFrom Watson_syndrome?oldid=679115166.
- Watson_syndrome isPrimaryTopicOf Watson_syndrome.
- Watson_syndrome name "Watson syndrome".