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Namespace Prefixes

PrefixIRI
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owlhttp://www.w3.org/2002/07/owl#
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Statements

Subject Item
n2:DOID_0110620
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_9562
rdfs:label
primary ciliary dyskinesia 35
wdrs:describedby
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obo:id
DOID:0110620
obo:hasDbXref
OMIM:617092
obo:hasExactSynonym
primary ciliary dyskinesia 35 with or without situs inversus CILD35
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozygous mutation in the TTC25 gene on chromosome 17q21.