This HTML5 document contains 145 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
dctermshttp://purl.org/dc/terms/
yago-reshttp://yago-knowledge.org/resource/
dbohttp://dbpedia.org/ontology/
foafhttp://xmlns.com/foaf/0.1/
n16https://global.dbpedia.org/id/
umbel-rchttp://umbel.org/umbel/rc/
yagohttp://dbpedia.org/class/yago/
dbthttp://dbpedia.org/resource/Template:
rdfshttp://www.w3.org/2000/01/rdf-schema#
freebasehttp://rdf.freebase.com/ns/
n10http://commons.wikimedia.org/wiki/Special:FilePath/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
wikipedia-enhttp://en.wikipedia.org/wiki/
dbphttp://dbpedia.org/property/
dbchttp://dbpedia.org/resource/Category:
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
wikidatahttp://www.wikidata.org/entity/
goldhttp://purl.org/linguistics/gold/
dbpedia-nlhttp://nl.dbpedia.org/resource/
dbrhttp://dbpedia.org/resource/

Statements

Subject Item
dbr:List_of_diseases_(K)
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Erythema
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Erythrokeratolysis_hiemalis
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
dbo:wikiPageRedirects
dbr:Keratolytic_winter_erythema
Subject Item
dbr:François_Renier_Duminy
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Oudtshoorn_disease
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
dbo:wikiPageRedirects
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Oudtshoorn_skin
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
dbo:wikiPageRedirects
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Keratolytic_winter_erythema
rdf:type
yago:IllHealth114052046 yago:Condition113920835 yago:GeneticDisease114151139 yago:State100024720 yago:Illness114061805 yago:AutosomalDominantDisease114162025 yago:Disease114070360 yago:WikicatGeneticDisordersWithOMIMButNoGene yago:PathologicalState114051917 yago:WikicatAutosomalDominantDisorders owl:Thing wikidata:Q12136 yago:PhysicalCondition114034177 yago:Attribute100024264 umbel-rc:AilmentCondition dbo:Disease yago:Abstraction100002137
rdfs:label
Keratolytic winter erythema Ziekte van Oudtshoorn
rdfs:comment
Keratolytic Winter erythema (also known as Oudtshoorn disease or Oudtshoorn skin) is a rare autosomal dominant skin disease of unknown cause which causes redness and peeling of the skin on the palms and soles. Onset, increased prominence and severity usually occurs during winter. It is a type of genodermatosis. The name "Oudtshoorn skin" derives from the town of Oudtshoorn in the Western Cape province of South Africa, where the disorder was first described. It is one of several genetic disorders known to be highly prevalent among the Afrikaner population. De huidziekte van Oudtshoorn of erythrokeratolysis hiemalis is een zeldzame erfelijke aandoening die in de winter huidschilfering aan handpalmen en voetzolen en erythemen veroorzaakt. De aanleiding hiervoor is een genafwijking op chromosoom 8 van het menselijk genoom. De ziekte was voorheen alleen in Zuid-Afrika bekend, waarvandaan de aandoening haar naam Oudtshoorn dankt. Er was ooit één blanke, onbekende, 'oprichter'. Een vermoeden van een Duitse oorsprong bleek ongegrond, daar Duitsers een andere mutatie blijken te bezitten.
foaf:name
Keratolytic winter erythema
dbp:name
Keratolytic winter erythema
foaf:depiction
n10:Autosomal_dominant_-_en.svg
dcterms:subject
dbc:Genodermatoses dbc:Rare_diseases dbc:Genetic_disorders_with_OMIM_but_no_gene dbc:Autosomal_dominant_disorders
dbo:wikiPageID
22828902
dbo:wikiPageRevisionID
1046617123
dbo:wikiPageWikiLink
dbr:Desquamation dbr:Torso dbr:CCL18 dbr:Cancer dbr:Lung_cancer dbr:MTMR8 dbr:Winter dbr:L-threonine_3-dehydrogenase dbr:Necrobiosis dbc:Genodermatoses dbr:Erythema dbr:Western_Cape dbr:Europe dbr:Mouse dbr:Ancestor dbr:Homology_(biology) dbr:Dominance_(genetics) dbr:Limb_(anatomy) dbr:Skin dbr:Lesion dbr:Transcription_(genetics) dbr:Microsatellite_(genetics) dbr:Founder_effect dbr:Integumentary_system dbc:Rare_diseases dbr:Oncogene dbr:Chromosome dbr:Chromosome_8_(human) dbr:South_Africa dbr:Gene dbr:BLK_(gene) dbr:Afrikaner dbr:Consanguinity dbr:Allele dbr:Buttocks dbr:Haplotype dbr:List_of_cutaneous_conditions dbr:Africa dbr:Hyperkeratosis dbr:Autosome dbr:Germany dbr:Skin_disease dbc:Genetic_disorders_with_OMIM_but_no_gene dbr:Genetic_diversity dbr:Cape_Province dbr:Inflammation dbr:Caucasian_race dbr:Denmark dbr:Dissection dbr:Mutation dbr:Cape_Town dbr:Breast_cancer dbr:Enzyme dbr:Loss_of_heterozygosity dbr:Heredity dbr:Myotubularin dbr:Kinship dbr:Sole_(foot) dbr:Oudtshoorn dbr:Hand dbr:Afrikaans dbc:Autosomal_dominant_disorders dbr:Malpighian_layer dbr:Stratum_corneum dbr:Genetic_disorder dbr:Genodermatosis dbr:Epidermis_(skin) dbr:Protein dbr:Candidate_gene
owl:sameAs
wikidata:Q1976193 freebase:m.06410rj n16:tb9z yago-res:Keratolytic_winter_erythema dbpedia-nl:Ziekte_van_Oudtshoorn
dbp:wikiPageUsesTemplate
dbt:Medical_resources dbt:Reflist dbt:Infobox_medical_condition_(new) dbt:Urticaria_and_erythema dbt:Empty_section dbt:Cn
dbo:thumbnail
n10:Autosomal_dominant_-_en.svg?width=300
dbp:icd
L53.8 695.9
dbp:meshid
536155.0
dbp:omim
148370
dbp:orphanet
50943
dbp:caption
Keratolytic Winter erythema has an autosomal dominant pattern of inheritance.
dbp:synonyms
KWE, Erythrokeratolysis hiemalis
dbo:abstract
Keratolytic Winter erythema (also known as Oudtshoorn disease or Oudtshoorn skin) is a rare autosomal dominant skin disease of unknown cause which causes redness and peeling of the skin on the palms and soles. Onset, increased prominence and severity usually occurs during winter. It is a type of genodermatosis. The name "Oudtshoorn skin" derives from the town of Oudtshoorn in the Western Cape province of South Africa, where the disorder was first described. It is one of several genetic disorders known to be highly prevalent among the Afrikaner population. De huidziekte van Oudtshoorn of erythrokeratolysis hiemalis is een zeldzame erfelijke aandoening die in de winter huidschilfering aan handpalmen en voetzolen en erythemen veroorzaakt. De aanleiding hiervoor is een genafwijking op chromosoom 8 van het menselijk genoom. De ziekte was voorheen alleen in Zuid-Afrika bekend, waarvandaan de aandoening haar naam Oudtshoorn dankt. Er was ooit één blanke, onbekende, 'oprichter'. Een vermoeden van een Duitse oorsprong bleek ongegrond, daar Duitsers een andere mutatie blijken te bezitten.
gold:hypernym
dbr:Disease
dbo:icd9
695.9
dbo:meshId
C536155
prov:wasDerivedFrom
wikipedia-en:Keratolytic_winter_erythema?oldid=1046617123&ns=0
dbo:wikiPageLength
16237
dbo:icd10
L53.8
dbo:omim
148370
dbo:orpha
50943
foaf:isPrimaryTopicOf
wikipedia-en:Keratolytic_winter_erythema
Subject Item
dbr:List_of_skin_conditions
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Erythrokeratolysis_hiemalis_ichthyosis
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
dbo:wikiPageRedirects
dbr:Keratolytic_winter_erythema
Subject Item
dbr:Oudtshoorn_skin_disease
dbo:wikiPageWikiLink
dbr:Keratolytic_winter_erythema
dbo:wikiPageRedirects
dbr:Keratolytic_winter_erythema
Subject Item
wikipedia-en:Keratolytic_winter_erythema
foaf:primaryTopic
dbr:Keratolytic_winter_erythema