Portal:RareDisease/News
From WikiPathways
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==== Explore rare disease pathways on WikiPathways: ==== | ==== Explore rare disease pathways on WikiPathways: ==== | ||
| - | * [[ | + | * [[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 disorders]] |
| - | * [[ | + | * [[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]] | ||
| + | * [[Pathway:WP4549|Fragile X Syndrome]] | ||
| + | * [[Pathway:WP4577|WDR45 autophagy related pathway]] | ||
| + | * [[Pathway:WP4312|Rett syndrome causing genes]] | ||
| + | * [[Pathway:WP3995|Prion disease pathway]] | ||
| + | * [[Pathway:WP3853|ERK Pathway in Huntington's Disease]] | ||
| + | * [[Pathway:WP4535|Envelope proteins and their potential roles in EDMD physiopathology]] | ||
| + | * [[Pathway:WP2371|Parkinsons Disease Pathway]] | ||
| + | * [[Pathway:WP2059|Alzheimers Disease]] | ||
Revision as of 07:15, 16 May 2019
Explore rare disease pathways on WikiPathways:
- MECP2 and Associated Rett Syndrome
- Amyotrophic lateral sclerosis (ALS)
- Fanconi Anemia Pathway
- The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome
- Lamin A-processing pathway
- Viral Acute Myocarditis
- Disorders of Phenylalanine and Tetrahydrobiopterin
- Tyrosine Metabolism
- Sulphur Amino Acids
- Disorders of Folate Metabolism and Transport
- MTHFR deficiency
- Vitamine B6-Dependent and Responsive Disorders
- Molybdenum (Moco) cofactor biosynthesis
- Cysteine and Methionine catabolism disorders
- Vitamin B12 Disorders
- Thiamine Disorders
- Disorders of the Krebs Cycle
- Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses
- Neurotransmitter Disorders
- Purine Disorders
- Pyrimidine Disorder
- Pathways Regulating Hippo Signaling
- po-Merlin Signaling Dysregulation
- Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases
- Cerebral Organic Acidurias
- Glycosylation and related congenital defects
- Metabolic pathway of LDL, HDL and TG
- Classical pathway of steroidogenesis, including diseases
- The alternative pathway of fetal androgen synthesis
- Fragile X Syndrome
- WDR45 autophagy related pathway
- Rett syndrome causing genes
- Prion disease pathway
- ERK Pathway in Huntington's Disease
- Envelope proteins and their potential roles in EDMD physiopathology
- Parkinsons Disease Pathway
- Alzheimers Disease
