Portal:RareDisease/FeaturedPathways
From WikiPathways
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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)}} | ||
- | + | |width=100px|{{#pwImage:Pathway:WP4156|250px||Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism}} | |
+ | |width=100px|{{#pwImage:Pathway:WP4506|250px||Tyrosine Metabolism}} | ||
|} | |} | ||
{| style="margin: 10px" | {| style="margin: 10px" | ||
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|width=100px|{{#pwImage:Pathway:WP4292|250px||Sulphur Amino Acids}} | |width=100px|{{#pwImage:Pathway:WP4292|250px||Sulphur Amino Acids}} | ||
|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)}} | ||
+ | |width=100px|{{#pwImage:Pathway:WP4228|250px||Vitamine B6-Dependent and Responsive Disorders}} | ||
|} | |} | ||
{| style="margin: 10px" | {| style="margin: 10px" | ||
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|width=100px|{{#pwImage:Pathway:WP4507|250px||Molybdenum (Moco) cofactor biosynthesis}} | |width=100px|{{#pwImage:Pathway:WP4507|250px||Molybdenum (Moco) cofactor biosynthesis}} | ||
|width=100px|{{#pwImage:Pathway:WP4504|250px||Cysteine and Methionine catabolism}} | |width=100px|{{#pwImage:Pathway:WP4504|250px||Cysteine and Methionine catabolism}} | ||
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|} | |} | ||
{| style="margin: 10px" | {| style="margin: 10px" | ||
- | |width=100px | + | |width=100px|{{#pwImage:Pathway:WP4236|250px||Disorders of the Krebs Cycle}} |
|width=100px|{{#pwImage:Pathway:WP4153|250px||Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses}} | |width=100px|{{#pwImage:Pathway:WP4153|250px||Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses}} | ||
|width=100px|{{#pwImage:Pathway:WP4220|250px||Neurotransmitter Disorders}} | |width=100px|{{#pwImage:Pathway:WP4220|250px||Neurotransmitter Disorders}} | ||
|width=100px|{{#pwImage:Pathway:WP4224|250px||Purine Disorders}} | |width=100px|{{#pwImage:Pathway:WP4224|250px||Purine Disorders}} | ||
+ | |} | ||
+ | {| style="margin: 10px" | ||
|width=100px|{{#pwImage:Pathway:WP4225|250px||Pyrimidine Disorders}} | |width=100px|{{#pwImage:Pathway:WP4225|250px||Pyrimidine Disorders}} | ||
|} | |} |
Revision as of 14:36, 30 January 2019
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List of featured pathways:
- Pathway:WP3584
- Pathway:WP2447
- Pathway:WP3569
- Pathway:WP4320
- Pathway:WP4299
- Pathway:WP4298
- Pathway:WP4156
- Pathway:WP4506
- Pathway:WP4292
- Pathway:WP4259
- Pathway:WP4288
- Pathway:WP4228
- Pathway:WP4507
- Pathway:WP4504
- Pathway:WP4271
- Pathway:WP4297
- Pathway:WP4236
- Pathway:WP4153
- Pathway:WP4220
- Pathway:WP4224
- Pathway:WP4225