glycogen storage disease II definition entry review update

Author: csbjohnson

src/ontology/doid-edit.owl

@@ -152329,7 +152329,7 @@ SubClassOf(obo:DOID_2751 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000149))
 
 # Class: obo:DOID_2752 (glycogen storage disease II)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007638) Annotation(oboInOwl:hasDbXref "url:http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_II") obo:IAO_0000115 obo:DOID_2752 "A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/6360103/") obo:IAO_0000115 obo:DOID_2752 "A glycogen storage disease characterized by cardiomyopathy and muscular hypotonia are the cardinal features.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2752 "GARD:5714")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2752 "ICD10CM:E74.02")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_2752 "MESH:D006009")
@@ -152347,6 +152347,7 @@ AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_2752 "acid maltase deficie
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_2752 "deficiency of glucoamylase")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_2752 "deficiency of maltase")
 AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_2752 "glycogen storage disease type II")
+AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_2752 "Pompe disease")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_2752 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_2752 "DOID:2752")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_2752 doid:DO_rare_slim)
@@ -152355,6 +152356,7 @@ AnnotationAssertion(rdfs:comment obo:DOID_2752 "OMIM mapping confirmed by DO. [S
 AnnotationAssertion(rdfs:label obo:DOID_2752 "glycogen storage disease II")
 SubClassOf(obo:DOID_2752 obo:DOID_2747)
 SubClassOf(obo:DOID_2752 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000148))
+SubClassOf(obo:DOID_2752 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0003593))
 
 # Class: obo:DOID_2753 (obsolete nervous system lysosomal storage disease)