Add primary ciliary dyskinesia 55

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -2268,6 +2268,7 @@ Declaration(Class(obo:DOID_0061222))
 Declaration(Class(obo:DOID_0061223))
 Declaration(Class(obo:DOID_0061224))
 Declaration(Class(obo:DOID_0061225))
+Declaration(Class(obo:DOID_0061226))
 Declaration(Class(obo:DOID_0070000))
 Declaration(Class(obo:DOID_0070001))
 Declaration(Class(obo:DOID_0070002))
@@ -44698,6 +44699,21 @@ AnnotationAssertion(skos:exactMatch obo:DOID_0061225 "ORDO:210115")
 SubClassOf(obo:DOID_0061225 obo:DOID_0051000)
 SubClassOf(obo:DOID_0061225 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
 
+# Class: obo:DOID_0061226 (primary ciliary dyskinesia 55)
+
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/31636325/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/40272718/") obo:IAO_0000115 obo:DOID_0061226 "A primary ciliary dyskinesia characterized by impairment of the function of the motile cilia of the airways, resulting in chronic respiratory tract infections and has_material_basis_in homozygous or compound heterozygous mutation in the CFAP221 gene on chromosome 2q14.")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061226 "GARD:341")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061226 "MIM:279000")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061226 "ORDO:3471")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0061226 "Azoospermia-sinopulmonary infections syndrome")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0061226 "Sinusitis-infertility syndrome")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0061226 "young syndrome")
+AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061226 "disease_ontology")
+AnnotationAssertion(oboInOwl:id obo:DOID_0061226 "DOID:0061226")
+AnnotationAssertion(rdfs:label obo:DOID_0061226 "primary ciliary dyskinesia 55")
+SubClassOf(obo:DOID_0061226 obo:DOID_9562)
+SubClassOf(obo:DOID_0061226 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
+
 # Class: obo:DOID_0070000 (3-methylglutaconic aciduria type 8)
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/27208207") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/27696117") obo:IAO_0000115 obo:DOID_0070000 "A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the HTRA2 gene on chromosome 2p13.")