Portal:Blau/CoveredPathways
From WikiPathways
| Chapter ed. 5 | Title | Links WP | Chapter ed. 4 | Status |
|---|---|---|---|---|
| 13 | Disorders of pyrimidine and purine metabolism | WP4225 and WP4224 | 41 | Approved |
| 16 | Disorders of glutathione metabolism | WP4518 | 42 | Approved |
| 19 | Disorders of monoamine metabolism | WP4220 | 31 | Approved |
| 20 | Disorders of phenylalanine and tetrahydrobiopterin metabolism | WP4156 | 1 | Approved |
| 21 | Disorders of tyrosine metabolism | WP4506 | 2 | Approved |
| 22 | Disorders of sulfur amino acid and sulfide metabolism | WP4292 | 3 | Approved |
| 23 | Disorders of branched-chain amino acid metabolism | WP4686 | 7 | In Progress |
| 26 | Disorders of glycine metabolism | WP4688 | 5 | In Progress |
| 28 | Disorders of cobalamin metabolism | WP4271 | 13 | Approved |
| 29 | Disorders of folate metabolism | WP4259 and WP4288 | 10 | Approved |
| 31 | Disorders of thiamine metabolism | WP4297 | 15 | Approved |
| 34 | Vitamin B6 -Dependent and Responsive Disorders | WP4228 | 11 | Approved |
| 35 | Disorders of molybdenum metabolism | WP4507 and WP4504 | 12 | Approved |
| 42 | Disorders of pyruvate and Krebs cycle metabolism | WP4236 | 20 | Approved |
| 53 | Disorders of lipoprotein metabolism | WP4522 | 43 | Approved |
| 55 | Disorders of steroid metabolism | WP4523 and WP4524 | 37 | Approved |
| 60 | Lysosomal storage disorders | WP4153 | 25 | Approved |
| 66 | Congenital disorders of N-linked and O-linked glycosylation | WP4521 | 30 | Approved |
| 69 | Cerebral organic acidurias | WP4519 | 8 | Approved |
Information on Pathway Curation:
This Table provides an overview of which chapters have been covered by WikiPathways. Approved pathways are coloured blue; pathways which still need work (however are a part of the database) are coloured orange.
Tip:
Click on the arrows behind the Table headers to sort this table based on Chapter number (edition 4 and 5 available), title, WikiPathways reference and Curation Status.
Pathway Visualisations
View all digitized Pathways from the Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases by Blau et al. see it on Scholia.
How to add a pathway to the portal
The list of Featured Pathways is not static and can be updated at any time. If you know of a pathway that should be added, please contact Denise Slenter.
