diff --git a/src/ontology/doid-edit.owl b/src/ontology/doid-edit.owl
index 9a487cd3..ff28b807 100644
--- a/src/ontology/doid-edit.owl
+++ b/src/ontology/doid-edit.owl
@@ -163448,7 +163448,7 @@ AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_4183 "NCI:C129722")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_4183 "SNOMEDCT_US_2023_03_01:190867002")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_4183 "UMLS_CUI:C0033835")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_4183 "Normocalcemic pseudohypoparathyroidism"@en)
-AnnotationAssertion(Annotation(rdfs:comment obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_4183 "PPHP"@en)
+AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_4183 "PPHP"@en)
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_4183 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_4183 "DOID:4183")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_4183 doid:DO_rare_slim)
@@ -163458,7 +163458,7 @@ SubClassOf(obo:DOID_4183 obo:DOID_4184)
 
 # Class: obo:DOID_4184 (pseudohypoparathyroidism)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref obo:ECO_0007646) Annotation(oboInOwl:hasDbXref "url:https://www.chop.edu/conditions-diseases/pseudohypoparathyroidism-php") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/books/NBK279165/") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/sites/books/NBK559141/") Annotation(rdfs:comment "url:https://pubmed.ncbi.nlm.nih.gov/27401862/") obo:IAO_0000115 obo:DOID_4184 "A metal metabolism disorder that is characterized by end-organ resistance to parathyroid hormone and/or a constellation of symptoms collectively termed Albright’s hereditary osteodystrophy, which include shortening and widening of long bones located_in the hand or located_in the foot along with short stature, obesity, and rounded face.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(dc:type obo:ECO_0007646) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/27401862/") Annotation(oboInOwl:hasDbXref "url:https://www.chop.edu/conditions-diseases/pseudohypoparathyroidism-php") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/books/NBK279165/") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/sites/books/NBK559141/") obo:IAO_0000115 obo:DOID_4184 "A metal metabolism disorder that is characterized by end-organ resistance to parathyroid hormone and/or a constellation of symptoms collectively termed Albright’s hereditary osteodystrophy, which include shortening and widening of long bones located_in the hand or located_in the foot along with short stature, obesity, and rounded face.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_4184 "GARD:10758")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_4184 "ICD10CM:E20.1")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_4184 "MESH:D011547")