Portal:RareDisease/FeaturedPathways
From WikiPathways
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Image does not exist MECP2 and Associated Rett Syndrome (Homo sapiens) |
Image does not exist Amyotrophic lateral sclerosis (ALS) (Homo sapiens) |
Image does not exist Fanconi Anemia Pathway (Homo sapiens) |
Image does not exist The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome (Homo sapiens) |
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Image does not exist Lamin A-processing pathway (Homo sapiens) |
Image does not exist Viral Acute Myocarditis (Homo sapiens) |
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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) |
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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 |
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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:
- 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
