Portal:RareDisease/BlauBookPathways

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* [[Pathway:WP4156]] - Chapter 1 "Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism"  
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* [[Pathway:WP4506]] - Chapter 2 "Tyrosine Metabolism"
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{{ #pathwayOfTheDay: {{LOCALDAYNAME}} {{LOCALDAY}} {{LOCALMONTHNAME}} {{LOCALYEAR}} | Portal:Disease/BlauBookPathways}}
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* [[Pathway:WP4292]] - Chapter 3 "Sulphur Amino Acids"
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|align="right"|[[Image:Blau_cover.jpg‎|170px]]
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|}
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<p>View all [[Portal:Disease/BlauBookPathways|Pathways]] digitized from [https://tools.wmflabs.org/scholia/work/Q54006412 Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases] by Blau ''et al.''</p>
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<b>How to add a pathway to the portal</b>
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* [[Pathway:WP4259]] - Chapter 10 "Disorders of Folate Metabolism and Transport"
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* [[Pathway:WP4288]] - Chapter 10 "MTHFR deficiency (additional pathway)"
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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 [mailto:denise.slenter@maastrichtuniversity contact Denise Slenter].
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{| style="margin: 10px"
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|width=100px; cell padding=50px|{{#pwImage:Pathway:WP4156|250px||Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism}}
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|width=100px|{{#pwImage:Pathway:WP4506|250px||Tyrosine Metabolism}}
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|width=100px|{{#pwImage:Pathway:WP4292|250px||Sulphur Amino Acids}}
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|width=100px|{{#pwImage:Pathway:WP4259|250px||Disorders of Folate Metabolism and Transport}}
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|width=100px|{{#pwImage:Pathway:WP4288|250px||MTHFR deficiency (additonal pathway)}}
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|}
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* [[Pathway:WP4228]] - Chapter 11 "Vitamine B6-Dependent and Responsive Disorders"
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* [[Pathway:WP4507]] - Chapter 12 "Molybdenum (Moco) cofactor biosynthesis"
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* [[Pathway:WP4504]] - Chapter 12 "Cysteine and Methionine catabolism"
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* [[Pathway:WP4271]] - Chapter 13 "Vitamin B12 Disorders"
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* [[Pathway:WP4297]] - Chapter 15 "Thiamine Disorders"
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{| style="margin: 10px"
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|width=100px; cell padding=50px|{{#pwImage:Pathway:WP4228|250px||Vitamine B6-Dependent and Responsive Disorders}}
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|width=100px|{{#pwImage:Pathway:WP4507|250px||Molybdenum (Moco) cofactor biosynthesis}}
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|width=100px|{{#pwImage:Pathway:WP4504|250px||Cysteine and Methionine catabolism}}
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|width=100px|{{#pwImage:Pathway:WP4271|250px||Vitamin B12 Disorders}}
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|width=100px|{{#pwImage:Pathway:WP4297|250px||Thiamine Disorders}}
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|}
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* [[Pathway:WP4236]] - Chapter 20 "Disorders of the Krebs Cycle" 
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* [[Pathway:WP4153]] - Chapter 25 "Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses (Sphingolipid degradation)"
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* [[Pathway:WP4220]] - Chapter 31 "Neurotransmitter Disorders" 
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* [[Pathway:WP4224]] - Chapter 41 "Purine Disorders"
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* [[Pathway:WP4225]] - Chapter 41 "Pyrimidine Disorders"
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{| style="margin: 10px"
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|width=100px; cell padding=50px|{{#pwImage:Pathway:WP4236|250px||Disorders of the Krebs Cycle}}
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|width=100px|{{#pwImage:Pathway:WP4153|250px||Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses (Sphingolipid degradation)}}
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|width=100px|{{#pwImage:Pathway:WP4220|250px||Neurotransmitter Disorders}}
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|width=100px|{{#pwImage:Pathway:WP4224|250px||Purine Disorders}}
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|width=100px|{{#pwImage:Pathway:WP4225|250px||Pyrimidine Disorders}}
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|}
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Pathways with kinetics data [coming soon!].
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* [[Pathway:WP4519]] - Chapter 8 "Cerebral Organic Acidurias, including diseases"
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* [[Pathway:WP4521]] - Chapter 30 "Glycosylation and related congenital defects."
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* [[Pathway:WP4523]] - Chapter 37 "Classical pathway of steroidogenesis, including diseases"
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* [[Pathway:WP4524]] - Chapter 37 "The alternative pathway of fetal androgen synthesis, including diseases"
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* [[Pathway:WP4518]] - Chapter 42 "Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases"
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* [[Pathway:WP4522]] - Chapter 43 "Metabolic pathway of LDL, HDL and TG, including diseases"
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{| style="margin: 10px"
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|width=60px; cell padding=50px|{{#pwImage:Pathway:WP4519|250px||Cerebral Organic Acidurias, including diseases}}
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|width=60px|{{#pwImage:Pathway:WP4521|230px||Glycosylation and related congenital defects.}}
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|width=60px|{{#pwImage:Pathway:WP4523|230px||Classical pathway of steroidogenesis, including diseases}}
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|width=60px|{{#pwImage:Pathway:WP4524|230px||The alternative pathway of fetal androgen synthesis, including diseases}}
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|width=60px|{{#pwImage:Pathway:WP4518|230px||Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases}}
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|width=60px|{{#pwImage:Pathway:WP4522|230px||Metabolic pathway of LDL, HDL and TG, including diseases}}
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|}

Revision as of 10:47, 7 May 2019

  • 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
Disorders of Folate Metabolism and Transport
Image does not exist
MTHFR deficiency (additonal pathway)
  • Pathway:WP4228 - Chapter 11 "Vitamine B6-Dependent and Responsive 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"
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


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"
  • Pathway:WP4522 - Chapter 43 "Metabolic pathway of LDL, HDL and TG, 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
Image does not exist
Metabolic pathway of LDL, HDL and TG, including diseases
Retrieved from "https://classic.wikipathways.org/index.php/Portal:RareDisease/BlauBookPathways"
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