Browsing pathways
Displaying pathways 23551 - 23575 of 48986 in total
Congenital Bile Acid Synthesis Defect Type II
Congenital Bile Acid Synthesis Defect Type III
Congenital disorder of glycosylation CDG-IId
Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
Congenital lactic acidosis
Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH
Corticosterone methyl oxidase I deficiency (CMO I)
Corticosterone methyl oxidase II deficiency - CMO II
Corticotropin Activation of Cortisol Production
Creatine deficiency, guanidinoacetate methyltransferase deficiency
Cyclizine H1-Antihistamine Action
Cyclophosphamide Action Pathway
Cyclophosphamide Metabolism Pathway
Cyclothiazide Action Pathway
Cyproheptadine H1-Antihistamine Action
Cystathionine Beta-Synthase Deficiency
Cysteine Metabolism
Cystinosis, ocular nonnephropathic
Cystinuria