Portal:IEM/CoveredPathways
From WikiPathways
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- | | ? || Leukotrienes || | + | | ? || Leukotrienes || [https://www.wikipathways.org/index.php/Pathway:WP5171 WP5171] || 38|| style="font-style: italic; color: blue;" | Approved |
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| ? || Disorders of Bile acid synthesis and biliary transport || [https://www.wikipathways.org/index.php/Pathway:WP5176 WP5176] || 34 || style="font-style: italic; color: blue;" | Approved | | ? || Disorders of Bile acid synthesis and biliary transport || [https://www.wikipathways.org/index.php/Pathway:WP5176 WP5176] || 34 || style="font-style: italic; color: blue;" | Approved |
Revision as of 08:28, 13 April 2022
Chapter ed. 5 | Title | Links WP | Chapter ed. 4 | Status | Diseases: x from ch. ed. 4 (+y) from other ch. |
---|---|---|---|---|---|
13 | Disorders of pyrimidine and purine metabolism | WP4225 and WP4224 | 41 | Approved | |
16 | Disorders of glutathione metabolism | WP4518 | 42 | Approved | |
17 | Disorders of ammonia detoxification | WP4595 | 4 | Approved | |
18 | Disorders of amino acid transport | WP5029 | 6 | In Progress | |
19 | Disorders of monoamine metabolism | WP4220 | 31 | Approved | |
20 | Disorders of phenylalanine and tetrahydrobiopterin metabolism | WP4156 | 1 | Approved | 7 (+3), non missing |
21 | Disorders of tyrosine metabolism | WP4506 | 2 | Approved | 5, non missing |
22 | Disorders of sulfur amino acid and sulfide metabolism | WP4292 | 3 | Approved | 7, non missing |
23 | Disorders of branched-chain amino acid metabolism | WP4686 | 7 | In Progress | |
26 | Disorders of glycine metabolism | Fig.5.1:WP5028, Fig.5.4: WP5026 | 5 | In Progress | |
26 | Disorders of glycine metabolism | Fig.5.2: WP4688 Fig.5.3: WP4157, | 5 | Approved | |
28 | Disorders of cobalamin metabolism | WP4271 | 13 | Approved | |
29 | Disorders of folate metabolism | WP4259 and WP4288 | 10 | Approved | |
30 | Disorders of biotin metabolism | WP5031 | 14 | Approved | |
31 | Disorders of thiamine metabolism | WP4297 | 15 | Approved | |
32 | Disorders of riboflavin metabolism | WP5037 | 16 | 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 | |
47 | Primary CoQ10 deficiencies | WP5037 | 16 | 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 and WP5030 | 8 & 9 | Approved | |
? | Disorders of phosphoinositide metabolism | WP4971 | ? | Approved | |
? | Oxysterols derived from cholesterol | WP4545 | ? | Approved | |
? | Leukotrienes | WP5171 | 38 | Approved | |
? | Disorders of Bile acid synthesis and biliary transport | WP5176 | 34 | Approved | |
? | Creatine disorders | 32 | In Progress | ||
? | Heme synthesis Defects and Porphyrias | WP5169 | 33 | Approved | |
? | Cholesterol synthesis disorders | WP5193 | 36 | Approved | |
? | Disorders of ketone body metabolism | 23 | In Progress | ||
? | Disorders of carbohydrate and glucose transport | 18 | In Progress | ||
? | Mitochondrial oxidative phosphorylation | 22 | In Progress | ||
? | Iron metabolism disorder | 40 | In Progress | ||
? | Mitochondrial fatty acid oxidation disorders | WP5123 | 17 | In Progress | |
? | Hyperoxalurias | WP5166 | 28 | In Progress | |
? | Disorders of copper metabolism | WP5189 | 39 | 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.