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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0111245
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_2121 n2:DOID_0080015 _:vb50944468
rdfs:label
palmoplantar keratoderma and congenital alopecia 2
wdrs:describedby
n7:doid.owl
obo:id
DOID:0111245
obo:hasDbXref
MESH:C535336 OMIM:212360 UMLS_CUI:C1859316 ORDO:1366
obo:hasExactSynonym
palmoplantar keratoderma and congenital alopecia, Wallis type PPKCA2 autosomal recessive palmoplantar hyperkeratosis and congenital alopecia autosomal recessive palmoplantar keratoderma and congenital alopecia PPK-CA, Wallis type CASS PPKCA Wallis type cataract-alopecia-sclerodactyly syndrome
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An ectodermal dysplasia characterized by autosomal recessive inheritance of alopecia, progressive palmoplantar hyperkeratosis resulting in sclerodactyly and usually associated with cataracts and pseudoainhum formation.
Subject Item
_:vb50944468
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:HP_0001197
wdrs:describedby
n7:doid.owl