Portal:RareDisease/News

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==== Explore rare disease pathways on WikiPathways: ====
==== Explore rare disease pathways on WikiPathways: ====
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* [[:Pathway:WP3584|MECP2 and Associated Rett Syndrome]]
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* [[Pathway:WP3584|MECP2 and Associated Rett Syndrome]]
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* [[:Pathway:WP2447|Amyotrophic lateral sclerosis (ALS) SOD1 - CHMP2B MODEL]]
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* [[Pathway:WP2447|Amyotrophic lateral sclerosis (ALS)]]
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* [[:Pathway:WP3569|Fanconi Anemia Pathway]]
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* [[Pathway:WP3569|Fanconi Anemia Pathway]]
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* [[:Pathway:WP4320|The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome]]
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* [[Pathway:WP4320|The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome]]
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* [[:Pathway:WP4299|Lamin A-processing pathway]]
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* [[Pathway:WP4299|Lamin A-processing pathway]]
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* [[:Pathway:WP4298|Viral Acute Myocarditis]]
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* [[Pathway:WP4298|Viral Acute Myocarditis]]
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* [[:Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin (BH4) Metabolism]]
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* [[Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin]]
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* [[:Pathway:WP4506|Tyrosine Metabolism]]
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* [[Pathway:WP4506|Tyrosine Metabolism]]
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* [[:Pathway:WP4292|Sulphur Amino Acids]]
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* [[Pathway:WP4292|Sulphur Amino Acids]]
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* [[:Pathway:WP4259|Disorders of Folate Metabolism and Transport]]
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* [[Pathway:WP4259|Disorders of Folate Metabolism and Transport]]
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* [[:Pathway:WP4288|MTHFR deficiency (additional pathway)]]
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* [[Pathway:WP4288|MTHFR deficiency]]
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* [[:Pathway:WP4228|Vitamine B6-Dependent and Responsive Disorders]]
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* [[Pathway:WP4228|Vitamine B6-Dependent and Responsive Disorders]]
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* [[:Pathway:WP4507|Molybdenum (Moco) cofactor biosynthesis]]
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* [[Pathway:WP4507|Molybdenum (Moco) cofactor biosynthesis]]
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* [[:Pathway:WP4504|Cysteine and Methionine catabolism]]
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* [[Pathway:WP4504|Cysteine and Methionine catabolism disorders]]
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* [[:Pathway:WP4271|Vitamin B12 Disorders]]
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* [[Pathway:WP4271|Vitamin B12 Disorders]]
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* [[:Pathway:WP4297|Thiamine Disorders]]
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* [[Pathway:WP4297|Thiamine Disorders]]
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* [[:Pathway:WP4236|Disorders of the Krebs Cycle]]
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* [[Pathway:WP4236|Disorders of the Krebs Cycle]]
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* [[:Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]]
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* [[Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]]
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* [[:Pathway:WP4220|Neurotransmitter Disorders]]
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* [[Pathway:WP4220|Neurotransmitter Disorders]]
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* [[:Pathway:WP4224|Purine Disorders]]
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* [[Pathway:WP4224|Purine Disorders]]
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* [[:Pathway:WP4225|Pyrimidine Disorders]]
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* [[Pathway:WP4225|Pyrimidine Disorder]]
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* [[Pathway:WP4540|Pathways Regulating Hippo Signaling]]
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* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
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* [[Pathway:WP4518|Gamma-Glutamyl Cycle for the biosynthesis and degradation of glutathione, including diseases]]
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* [[Pathway:WP4519|Cerebral Organic Acidurias]]
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* [[Pathway:WP4521|Glycosylation and related congenital defects]]
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* [[Pathway:WP4522|Metabolic pathway of LDL, HDL and TG]]
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* [[Pathway:WP4523|Classical pathway of steroidogenesis, including diseases]]
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* [[Pathway:WP4524|The alternative pathway of fetal androgen synthesis]]
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* [[Pathway:WP4549|Fragile X Syndrome]]
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* [[Pathway:WP4577|WDR45 autophagy related pathway]]
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* [[Pathway:WP4312|Rett syndrome causing genes]]
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* [[Pathway:WP3995|Prion disease pathway]]
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* [[Pathway:WP3853|ERK Pathway in Huntington's Disease]]
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* [[Pathway:WP4535|Envelope proteins and their potential roles in EDMD physiopathology]]
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* [[Pathway:WP2371|Parkinsons Disease Pathway]]
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* [[Pathway:WP2059|Alzheimers Disease]]

Revision as of 07:15, 16 May 2019

Explore rare disease pathways on WikiPathways:

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