Found metabolites without interaction: 3
https://identifiers.org/wikipathways/WP5173 has an metabolite not linked to an interaction: Glucose-6-phosphate
https://identifiers.org/wikipathways/WP5173 has an metabolite not linked to an interaction: UDP-galactose
https://identifiers.org/wikipathways/WP5173 has an metabolite not linked to an interaction: Glycogen
Unexpected data source for the metabolic conversion: 1
https://identifiers.org/wikipathways/WP5173 http://rdf.wikipathways.org/Pathway/WP5173_r136172/WP/Interaction/e0131 Wikidata Q22281942
Interactions found that involve Labels: 13
http://classic.wikipathways.org/instance/WP5173_r136172 "Fanconi-Bickel syndrome" with graphId fd3d0
http://classic.wikipathways.org/instance/WP5173_r136172 "Uridine diphosphate
galactose-4-epimerase
deficiency" with graphId c9ff6
http://classic.wikipathways.org/instance/WP5173_r136172 "Congenital disorder of glycosylation,
type It" with graphId de139
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage
disease IV" with graphId aaa50
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage disease 0, muscle" with graphId fbaa3
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage disease XV" with graphId abc2c
http://classic.wikipathways.org/instance/WP5173_r136172 "Galactosaemia" with graphId a8706
http://classic.wikipathways.org/instance/WP5173_r136172 "Intestinal glucose-galactose
malabsorption" with graphId d61c1
http://classic.wikipathways.org/instance/WP5173_r136172 "Polyglucosan body myopathy 2" with graphId b5440
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage
disease VI" with graphId ae5e6
http://classic.wikipathways.org/instance/WP5173_r136172 "Galactokinase deficiency" with graphId d2625
http://classic.wikipathways.org/instance/WP5173_r136172 "Glycogen storage disease 0, liver" with graphId f124e
http://classic.wikipathways.org/instance/WP5173_r136172 "Polyglucosan body neuropathy" with graphId eba21