Portal:IEM/FeaturedPathways
From WikiPathways
(Difference between revisions)
(New page: * Pathway:WP4156 - Chapter 1 "Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism" * Pathway:WP4506 - Chapter 2 "Tyrosine Metabolism" * Pathway:WP4292 - Chapte...) |
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+ | Note: these pathways are named after version 4 of the book, and might deviate (significantly) from version 5 names. | ||
+ | For an overview, please see the [https://www.wikipathways.org/index.php/Portal:IEM Covered Pathways] section on the main portal page. | ||
+ | |||
* [[Pathway:WP4156]] - Chapter 1 "Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism" | * [[Pathway:WP4156]] - Chapter 1 "Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism" | ||
* [[Pathway:WP4506]] - Chapter 2 "Tyrosine Metabolism" | * [[Pathway:WP4506]] - Chapter 2 "Tyrosine Metabolism" | ||
* [[Pathway:WP4292]] - Chapter 3 "Sulphur Amino Acids" | * [[Pathway:WP4292]] - Chapter 3 "Sulphur Amino Acids" | ||
+ | * [[Pathway:WP4595]] - Chapter 4 "Hyperammonemias and related disorders" | ||
* [[Pathway:WP4259]] - Chapter 10 "Disorders of Folate Metabolism and Transport" | * [[Pathway:WP4259]] - Chapter 10 "Disorders of Folate Metabolism and Transport" | ||
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|width=100px|{{#pwImage:Pathway:WP4506|250px||Tyrosine Metabolism}} | |width=100px|{{#pwImage:Pathway:WP4506|250px||Tyrosine Metabolism}} | ||
|width=100px|{{#pwImage:Pathway:WP4292|250px||Sulphur Amino Acids}} | |width=100px|{{#pwImage:Pathway:WP4292|250px||Sulphur Amino Acids}} | ||
+ | |width=100px|{{#pwImage:Pathway:WP4595|250px||Hyperammonemias and related disorders}} | ||
|width=100px|{{#pwImage:Pathway:WP4259|250px||Disorders of Folate Metabolism and Transport}} | |width=100px|{{#pwImage:Pathway:WP4259|250px||Disorders of Folate Metabolism and Transport}} | ||
|width=100px|{{#pwImage:Pathway:WP4288|250px||MTHFR deficiency (additonal pathway)}} | |width=100px|{{#pwImage:Pathway:WP4288|250px||MTHFR deficiency (additonal pathway)}} |
Revision as of 11:13, 18 December 2020
Note: these pathways are named after version 4 of the book, and might deviate (significantly) from version 5 names. For an overview, please see the Covered Pathways section on the main portal page.
- Pathway:WP4156 - Chapter 1 "Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism"
- Pathway:WP4506 - Chapter 2 "Tyrosine Metabolism"
- Pathway:WP4292 - Chapter 3 "Sulphur Amino Acids"
- Pathway:WP4595 - Chapter 4 "Hyperammonemias and related disorders"
- Pathway:WP4259 - Chapter 10 "Disorders of Folate Metabolism and Transport"
- Pathway:WP4288 - Chapter 10 "MTHFR deficiency (additional pathway)"
Image does not exist Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism |
Image does not exist Tyrosine Metabolism |
Image does not exist Sulphur Amino Acids |
Image does not exist Hyperammonemias and related disorders |
Image does not exist Disorders of Folate Metabolism and Transport |
Image does not exist MTHFR deficiency (additonal pathway) |
- Pathway:WP4228 - Chapter 11 "Vitamine B6-Dependent and Responsive Disorders"
- Pathway:WP4507 - Chapter 12 "Molybdenum (Moco) cofactor biosynthesis"
- Pathway:WP4504 - Chapter 12 "Cysteine and Methionine catabolism"
- Pathway:WP4271 - Chapter 13 "Vitamin B12 Disorders"
- Pathway:WP4297 - Chapter 15 "Thiamine Disorders"
Image does not exist Vitamine B6-Dependent and Responsive Disorders |
Image does not exist Molybdenum (Moco) cofactor biosynthesis |
Image does not exist Cysteine and Methionine catabolism |
Image does not exist Vitamin B12 Disorders |
Image does not exist Thiamine Disorders |
- Pathway:WP4236 - Chapter 20 "Disorders of the Krebs Cycle"
- Pathway:WP4153 - Chapter 25 "Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses (Sphingolipid degradation)"
- Pathway:WP4220 - Chapter 31 "Neurotransmitter Disorders"
- Pathway:WP4224 - Chapter 41 "Purine Disorders"
- Pathway:WP4225 - Chapter 41 "Pyrimidine Disorders"
- Pathway:WP4522 - Chapter 43 "Metabolic pathway of LDL, HDL and TG, including diseases"
Image does not exist Disorders of the Krebs Cycle |
Image does not exist Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses (Sphingolipid degradation) |
Image does not exist Neurotransmitter Disorders |
Image does not exist Purine Disorders |
Image does not exist Pyrimidine Disorders |
Image does not exist Metabolic pathway of LDL, HDL and TG, including diseases |
Pathways with kinetics data [coming soon!].
- Pathway:WP4519 - Chapter 8 "Cerebral Organic Acidurias, including diseases"
- Pathway:WP4521 - Chapter 30 "Glycosylation and related congenital defects."
- Pathway:WP4523 - Chapter 37 "Classical pathway of steroidogenesis, including diseases"
- Pathway:WP4524 - Chapter 37 "The alternative pathway of fetal androgen synthesis, including diseases"
- Pathway:WP4518 - Chapter 42 "Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases"
Image does not exist Cerebral Organic Acidurias, including diseases |
Image does not exist Glycosylation and related congenital defects. |
Image does not exist Classical pathway of steroidogenesis, including diseases |
Image does not exist The alternative pathway of fetal androgen synthesis, including diseases |
Image does not exist Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases |