Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Schöpf–Schulz–Passarge_syndrome> ?p ?o }
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- Schöpf–Schulz–Passarge_syndrome abstract "Schöpf–Schulz–Passarge syndrome (also known as \"Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis\") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.It was characterized in 1971.It has been associated with WNT10A.".
- Schöpf–Schulz–Passarge_syndrome icd10 "Q82.8".
- Schöpf–Schulz–Passarge_syndrome omim "224750".
- Schöpf–Schulz–Passarge_syndrome wikiPageID "21522840".
- Schöpf–Schulz–Passarge_syndrome wikiPageLength "2319".
- Schöpf–Schulz–Passarge_syndrome wikiPageOutDegree "8".
- Schöpf–Schulz–Passarge_syndrome wikiPageRevisionID "679043963".
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink Category:Palmoplantar_keratodermas.
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink Dominance_(genetics).
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink List_of_cutaneous_conditions.
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink List_of_cutaneous_neoplasms_associated_with_systemic_syndromes.
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink List_of_dental_abnormalities_associated_with_cutaneous_conditions.
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink Palmoplantar_keratoderma.
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLink WNT10A.
- Schöpf–Schulz–Passarge_syndrome wikiPageWikiLinkText "Schöpf–Schulz–Passarge syndrome".
- Schöpf–Schulz–Passarge_syndrome icd "Q82.8".
- Schöpf–Schulz–Passarge_syndrome name "Schöpf–Schulz–Passarge syndrome".
- Schöpf–Schulz–Passarge_syndrome omim "224750".
- Schöpf–Schulz–Passarge_syndrome wikiPageUsesTemplate Template:Cutaneous-condition-stub.
- Schöpf–Schulz–Passarge_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Schöpf–Schulz–Passarge_syndrome wikiPageUsesTemplate Template:Reflist.
- Schöpf–Schulz–Passarge_syndrome wikiPageUsesTemplate Template:Rp.
- Schöpf–Schulz–Passarge_syndrome subject Category:Palmoplantar_keratodermas.
- Schöpf–Schulz–Passarge_syndrome hypernym Condition.
- Schöpf–Schulz–Passarge_syndrome type Disease.
- Schöpf–Schulz–Passarge_syndrome type Diacritic.
- Schöpf–Schulz–Passarge_syndrome type Redirect.
- Schöpf–Schulz–Passarge_syndrome type Thing.
- Schöpf–Schulz–Passarge_syndrome type Q12136.
- Schöpf–Schulz–Passarge_syndrome comment "Schöpf–Schulz–Passarge syndrome (also known as \"Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis\") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.It was characterized in 1971.It has been associated with WNT10A.".
- Schöpf–Schulz–Passarge_syndrome label "Schöpf–Schulz–Passarge syndrome".
- Schöpf–Schulz–Passarge_syndrome sameAs Q7433355.
- Schöpf–Schulz–Passarge_syndrome sameAs Schöpf-Schulz-Passarge-Syndrom.
- Schöpf–Schulz–Passarge_syndrome sameAs m.05h35qv.
- Schöpf–Schulz–Passarge_syndrome sameAs Q7433355.
- Schöpf–Schulz–Passarge_syndrome wasDerivedFrom Schöpf–Schulz–Passarge_syndrome?oldid=679043963.
- Schöpf–Schulz–Passarge_syndrome isPrimaryTopicOf Schöpf–Schulz–Passarge_syndrome.
- Schöpf–Schulz–Passarge_syndrome name "Schöpf–Schulz–Passarge syndrome".