<http://purl.obolibrary.org/obo/DOID_0110595>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance and ciliopathy with some type of intestinal atresia, variable ocular abnormalities, microcephaly, and has_material_basis_in compound heterozygous mutation in the CENPF gene on chromosome 1q41."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"apple peel syndrome with microcephaly and ocular anomalies"@en .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_9562> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q87.8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:243605"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CILD31"@en .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"primary ciliary dyskinesia 31"@en .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"jejunal atresia with microcephaly and ocular anomalies"@en .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.w3.org/2000/01/rdf-schema#label>	"Stromme syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110595>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110595"^^<http://www.w3.org/2001/XMLSchema#string> .