SMPDB

NOTE: In this table, similarly named pathways have been grouped together. Groupings are represented by a single primary pathway, hence the table name, which has a clickable pathway name displayed in blue text. For instance, the two pathways Cardiolipin Biosynthesis CL(16:0/16:0/16:0/16:0) and Cardiolipin Biosynthesis CL(16:0/16:0/16:0/18:0) would be grouped under the primary pathway Cardiolipin Biosynthesis.

Showing 201 - 220 of 914 primary pathways

SMPDB ID	Pathway	View Link
SMP0000262	Clomocycline Action Pathway	View Pathway
SMP0000260	Clopidogrel Action Pathway	View Pathway
SMP0000610	Clopidogrel Metabolism Pathway	View Pathway
SMP0000586	Coagulation	View Pathway
SMP0000395	Cocaine Action Pathway	View Pathway
SMP0000405	Codeine Action Pathway	View Pathway
SMP0000621	Codeine Metabolism Pathway	View Pathway
SMP0063814	Complement Pathway	View Pathway
SMP0000314	Congenital Bile Acid Synthesis Defect Type II	View Pathway
SMP0000318	Congenital Bile Acid Synthesis Defect Type III	View Pathway
SMP0000579	Congenital Disorder of Glycosylation CDG-IId	View Pathway
SMP0000345	Congenital Erythropoietic Porphyria (CEP) or Gunther Disease	View Pathway
SMP0000546	Congenital Lactic Acidosis	View Pathway
SMP0000371	Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH	View Pathway
SMP0000577	Corticosterone Methyl Oxidase I Deficiency (CMO I)	View Pathway
SMP0000578	Corticosterone Methyl Oxidase II Deficiency (CMO II)	View Pathway
SMP0000310	Corticotropin Activation of Cortisol Production	View Pathway
SMP0000504	Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency	View Pathway
SMP0064625	CXCR4 Signaling Pathway	View Pathway
SMP0058923	Cyclizine H1-Antihistamine Action	View Pathway

Showing 201 - 220 of 914 primary pathways

Table of Primary Pathways

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Clomocycline Action Pathway

Clopidogrel Action Pathway

Clopidogrel Metabolism Pathway

Coagulation

Cocaine Action Pathway

Codeine Action Pathway

Codeine Metabolism Pathway

Complement Pathway

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

CXCR4 Signaling Pathway

Cyclizine H1-Antihistamine Action