Add Carey-Fineman-Ziter syndrome 1, Carey-Fineman-Ziter syndrome 2 and add Carey-Fineman-Ziter syndrome xref

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -2146,6 +2146,7 @@ Declaration(Class(obo:DOID_0061112))
 Declaration(Class(obo:DOID_0061113))
 Declaration(Class(obo:DOID_0061114))
 Declaration(Class(obo:DOID_0061115))
+Declaration(Class(obo:DOID_0061116))
 Declaration(Class(obo:DOID_0070000))
 Declaration(Class(obo:DOID_0070001))
 Declaration(Class(obo:DOID_0070002))
@@ -43767,6 +43768,18 @@ AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061115 "disease_ontology"
 AnnotationAssertion(oboInOwl:id obo:DOID_0061115 "DOID:0061115")
 AnnotationAssertion(rdfs:label obo:DOID_0061115 "Carey-Fineman-Ziter syndrome 1")
 SubClassOf(obo:DOID_0061115 obo:DOID_0080194)
+SubClassOf(obo:DOID_0061115 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
+
+# Class: obo:DOID_0061116 (Carey-Fineman-Ziter syndrome 2)
+
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/39668186/") obo:IAO_0000115 obo:DOID_0061116 "A Carey-Fineman-Ziter syndrome characterized by motor developmental delay, facial weakness, hypotonia, growth restriction, feeding difficulties, and velopharyngeal insufficiency that has_material_basis_inhomozygous mutation in MYMX gene on chromosome 6p21.")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0061116 "MIM:619941")
+AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0061116 "CFZS2")
+AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061116 "disease_ontology")
+AnnotationAssertion(oboInOwl:id obo:DOID_0061116 "DOID:0061116")
+AnnotationAssertion(rdfs:label obo:DOID_0061116 "Carey-Fineman-Ziter syndrome 2")
+SubClassOf(obo:DOID_0061116 obo:DOID_0080194)
+SubClassOf(obo:DOID_0061116 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
 
 # Class: obo:DOID_0070000 (3-methylglutaconic aciduria type 8)
 
@@ -54770,6 +54783,7 @@ SubClassOf(obo:DOID_0080193 ObjectSomeValuesFrom(obo:RO_0002452 obo:SYMP_0020022
 
 AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/28681861") Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/254940?search=254940&highlight=254940") obo:IAO_0000115 obo:DOID_0080194 "A syndrome characterized by hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre Robin complex (micrognathia, glossoptosis, and high-arched or cleft palate), delayed motor milestones, and failure to thrive.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080194 "GARD:3889")
+AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080194 "MIM:PS254940")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080194 "ORDO:1358")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080194 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0080194 "DOID:0080194")