Portal:IEM/CoveredPathways

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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 41 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.

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