Portal:RareDisease/FeaturedPathways

From WikiPathways

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(New page: {| style="margin: 10px" |width=100px; cell padding=50px|{{#pwImage:Pathway:WP3584|250px||MECP2 and Associated Rett Syndrome (Homo sapiens)}} |width=100px|{{#pwImage:Pathway:WP2447|250px||A...)
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|width=100px|{{#pwImage:Pathway:WP4299|250px||Lamin A-processing pathway (Homo sapiens)}}
|width=100px|{{#pwImage:Pathway:WP4299|250px||Lamin A-processing pathway (Homo sapiens)}}
|width=100px|{{#pwImage:Pathway:WP4298|250px||Viral Acute Myocarditis (Homo sapiens)}}
|width=100px|{{#pwImage:Pathway:WP4298|250px||Viral Acute Myocarditis (Homo sapiens)}}
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|}
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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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{| 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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{| 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}}
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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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* [[Pathway:WP4299]]
* [[Pathway:WP4299]]
* [[Pathway:WP4298]]
* [[Pathway:WP4298]]
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* [[Pathway:WP4156]]
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* [[Pathway:WP4506]]
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* [[Pathway:WP4292]]
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* [[Pathway:WP4259]]
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* [[Pathway:WP4288]]
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* [[Pathway:WP4228]]
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* [[Pathway:WP4507]]
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* [[Pathway:WP4504]]
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* [[Pathway:WP4271]]
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* [[Pathway:WP4297]]
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* [[Pathway:WP4236]]
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* [[Pathway:WP4153]]
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* [[Pathway:WP4220]]
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* [[Pathway:WP4224]]
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* [[Pathway:WP4225]]

Revision as of 14:28, 30 January 2019

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MECP2 and Associated Rett Syndrome (Homo sapiens)
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Amyotrophic lateral sclerosis (ALS) (Homo sapiens)
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Fanconi Anemia Pathway (Homo sapiens)
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The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome (Homo sapiens)
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Lamin A-processing pathway (Homo sapiens)
Image does not exist
Viral Acute Myocarditis (Homo sapiens)
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)
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
Image does not exist
Disorders of the Krebs Cycle
Image does not exist
Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses
Image does not exist
Neurotransmitter Disorders
Image does not exist
Purine Disorders
Image does not exist
Pyrimidine Disorders

List of featured pathways:

Retrieved from "https://classic.wikipathways.org/index.php/Portal:RareDisease/FeaturedPathways"
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