Portal:RareDisease/FeaturedPathways
From WikiPathways
(Difference between revisions)
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List of featured pathways: | List of featured pathways: | ||
* [[Pathway:WP3584]] - MECP2 and Associated Rett Syndrome | * [[Pathway:WP3584]] - MECP2 and Associated Rett Syndrome | ||
| - | * [[Pathway:WP2447]] | + | * [[Pathway:WP2447]] - Amyotrophic lateral sclerosis (ALS) |
| - | * [[Pathway:WP3569]] | + | * [[Pathway:WP3569]] - Fanconi Anemia Pathway |
| - | * [[Pathway:WP4320]] | + | * [[Pathway:WP4320]] - The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome |
| - | * [[Pathway:WP4299]] | + | * [[Pathway:WP4299]] - Lamin A-processing pathway |
| - | * [[Pathway:WP4298]] | + | * [[Pathway:WP4298]] - Viral Acute Myocarditis |
| - | * [[Pathway:WP4156]] | + | * [[Pathway:WP4156]] - Disorders of Phenylalanine and Tetrahydrobiopterin |
| - | * [[Pathway:WP4506]] | + | * [[Pathway:WP4506]] - Tyrosine Metabolism |
| - | * [[Pathway:WP4292]] | + | * [[Pathway:WP4292]] - Sulphur Amino Acids |
| - | * [[Pathway:WP4259]] | + | * [[Pathway:WP4259]] - Disorders of Folate Metabolism and Transport |
| - | * [[Pathway:WP4288]] | + | * [[Pathway:WP4288]] - MTHFR deficiency |
| - | * [[Pathway:WP4228]] | + | * [[Pathway:WP4228]] - Vitamine B6-Dependent and Responsive Disorders |
| - | * [[Pathway:WP4507]] | + | * [[Pathway:WP4507]] - Molybdenum (Moco) cofactor biosynthesis |
| - | * [[Pathway:WP4504]] | + | * [[Pathway:WP4504]] - Cysteine and Methionine catabolism |
| - | * [[Pathway:WP4271]] | + | * [[Pathway:WP4271]] - Vitamin B12 Disorders |
| - | * [[Pathway:WP4297]] | + | * [[Pathway:WP4297]] - Thiamine Disorders |
| - | * [[Pathway:WP4236]] | + | * [[Pathway:WP4236]] - Disorders of the Krebs Cycle |
| - | * [[Pathway:WP4153]] | + | * [[Pathway:WP4153]] - Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses |
| - | * [[Pathway:WP4220]] | + | * [[Pathway:WP4220]] - Neurotransmitter Disorders |
| - | * [[Pathway:WP4224]] | + | * [[Pathway:WP4224]] - Purine Disorders |
| - | * [[Pathway:WP4225]] | + | * [[Pathway:WP4225]] - Pyrimidine Disorder |
| - | * [[Pathway:WP4540]] | + | * [[Pathway:WP4540]] - Pathways Regulating Hippo Signaling |
| - | * [[Pathway:WP4541]] | + | * [[Pathway:WP4541]] - po-Merlin Signaling Dysregulation |
| - | * [[Pathway:WP4518]] | + | * [[Pathway:WP4518]] - Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases |
| - | * [[Pathway:WP4519]] | + | * [[Pathway:WP4519]] - Cerebral Organic Acidurias |
| - | * [[Pathway:WP4521]] | + | * [[Pathway:WP4521]] - Glycosylation and related congenital defects |
| - | * [[Pathway:WP4522]] | + | * [[Pathway:WP4522]] - Metabolic pathway of LDL, HDL and TG |
| - | * [[Pathway:WP4523]] | + | * [[Pathway:WP4523]] - Classical pathway of steroidogenesis, including diseases |
| - | * [[Pathway:WP4524]] | + | * [[Pathway:WP4524]] - The alternative pathway of fetal androgen synthesis |
Revision as of 08:03, 15 May 2019
|
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) |
|
Image does not exist 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 |
Image does not exist Pathways Regulating Hippo Signaling |
Image does not exist po-Merlin Signaling Dysregulation |
List of featured pathways:
- Pathway:WP3584 - MECP2 and Associated Rett Syndrome
- Pathway:WP2447 - Amyotrophic lateral sclerosis (ALS)
- Pathway:WP3569 - Fanconi Anemia Pathway
- Pathway:WP4320 - The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome
- Pathway:WP4299 - Lamin A-processing pathway
- Pathway:WP4298 - Viral Acute Myocarditis
- Pathway:WP4156 - Disorders of Phenylalanine and Tetrahydrobiopterin
- Pathway:WP4506 - Tyrosine Metabolism
- Pathway:WP4292 - Sulphur Amino Acids
- Pathway:WP4259 - Disorders of Folate Metabolism and Transport
- Pathway:WP4288 - MTHFR deficiency
- Pathway:WP4228 - Vitamine B6-Dependent and Responsive Disorders
- Pathway:WP4507 - Molybdenum (Moco) cofactor biosynthesis
- Pathway:WP4504 - Cysteine and Methionine catabolism
- Pathway:WP4271 - Vitamin B12 Disorders
- Pathway:WP4297 - Thiamine Disorders
- Pathway:WP4236 - Disorders of the Krebs Cycle
- Pathway:WP4153 - Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses
- Pathway:WP4220 - Neurotransmitter Disorders
- Pathway:WP4224 - Purine Disorders
- Pathway:WP4225 - Pyrimidine Disorder
- Pathway:WP4540 - Pathways Regulating Hippo Signaling
- Pathway:WP4541 - po-Merlin Signaling Dysregulation
- Pathway:WP4518 - Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases
- Pathway:WP4519 - Cerebral Organic Acidurias
- Pathway:WP4521 - Glycosylation and related congenital defects
- Pathway:WP4522 - Metabolic pathway of LDL, HDL and TG
- Pathway:WP4523 - Classical pathway of steroidogenesis, including diseases
- Pathway:WP4524 - The alternative pathway of fetal androgen synthesis
