Portal:RareDisease/News

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Current revision (11:40, 4 May 2023) (view source)
 
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==== Explore rare disease pathways on WikiPathways: ====
==== Explore rare disease pathways on WikiPathways: ====
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Overview table here: [https://www.wikipathways.org/index.php?title=Special:CurationTags&showPathwaysFor=Curation%3ARareDiseases]
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Overview table here: [https://classic.wikipathways.org/index.php?title=Special:CurationTags&showPathwaysFor=Curation%3ARareDiseases]
* [[Pathway:WP3584|MECP2 and Associated Rett Syndrome]]
* [[Pathway:WP3584|MECP2 and Associated Rett Syndrome]]
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* [[Pathway:WP3569|Fanconi Anemia Pathway]]
* [[Pathway:WP3569|Fanconi Anemia Pathway]]
* [[Pathway:WP4298|Viral Acute Myocarditis]]
* [[Pathway:WP4298|Viral Acute Myocarditis]]
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* [[Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]]
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* [[Pathway:WP4153|Degradation pathway of sphingolipids, including diseases]]
* [[Pathway:WP4540|Pathways Regulating Hippo Signaling]]
* [[Pathway:WP4540|Pathways Regulating Hippo Signaling]]
* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
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* [[Pathway:WP4947|Nitric oxide metabolism in cystic fibrosis]]
* [[Pathway:WP4947|Nitric oxide metabolism in cystic fibrosis]]
* [[Pathway:WP5087|Malignant pleural mesothelioma]]
* [[Pathway:WP5087|Malignant pleural mesothelioma]]
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* [[Pathway:WP4804|Cholesterol biosynthesis with skeletal dysplasias]]
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* [[Pathway:WP5114|Nucleotide excision repair in xeroderma pigmentosum]]
Laminopathy pathways
Laminopathy pathways
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* [[Pathway:WP4871|Kisspeptin/Kisspeptin Receptor System in the Ovary]]
* [[Pathway:WP4871|Kisspeptin/Kisspeptin Receptor System in the Ovary]]
* [[Pathway:WP4835|Peroxiredoxin 2 induced ovarian failure]]
* [[Pathway:WP4835|Peroxiredoxin 2 induced ovarian failure]]
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* [[Pathway:WP5074|Kallmann syndrome]]
Copy number variation syndromes (CNVs) - duplications or deletions
Copy number variation syndromes (CNVs) - duplications or deletions
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* [[Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin]]
* [[Pathway:WP4156|Disorders of Phenylalanine and Tetrahydrobiopterin]]
* [[Pathway:WP4506|Tyrosine Metabolism]]
* [[Pathway:WP4506|Tyrosine Metabolism]]
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* [[Pathway:WP4292|Sulphur Amino Acids]]
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* [[Pathway:WP4292|Methionine metabolism leading to sulfur amino acids and related disorders]]
* [[Pathway:WP4259|Disorders of Folate Metabolism and Transport]]
* [[Pathway:WP4259|Disorders of Folate Metabolism and Transport]]
* [[Pathway:WP4288|MTHFR deficiency]]
* [[Pathway:WP4288|MTHFR deficiency]]

Current revision

Explore rare disease pathways on WikiPathways:

Overview table here: [1]

Laminopathy pathways

CAKUT (congenital anomalies of the kidney and urinary tract)

Disorders of sex development and fertility

Copy number variation syndromes (CNVs) - duplications or deletions

Lipodystrophy, dyslipidemia and hyperlipidemia

Inborn errors of metabolism

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