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* [[Pathway:WP3569|Fanconi Anemia Pathway]]
* [[Pathway:WP3569|Fanconi Anemia Pathway]]
* [[Pathway:WP4298|Viral Acute Myocarditis]]
* [[Pathway:WP4298|Viral Acute Myocarditis]]
-
* [[Pathway:WP4153|Lysosomal Storage Disorders Including Neuronal Ceroid Lipofuscinoses]]
+
* [[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: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]]
+
* [[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]]

Revision as of 13:52, 28 May 2021

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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