Portal:RareDisease/News

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* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
* [[Pathway:WP4541|po-Merlin Signaling Dysregulation]]
* [[Pathway:WP4549|Fragile X Syndrome]]
* [[Pathway:WP4549|Fragile X Syndrome]]
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* [[Pathway:WP4577|WDR45 autophagy related pathway]]
+
* [[Pathway:WP4577|Neurodegeneration with brain iron accumulation (NBIA) subtypes pathway]]
* [[Pathway:WP3995|Prion disease pathway]]
* [[Pathway:WP3995|Prion disease pathway]]
* [[Pathway:WP3853|ERK Pathway in Huntington's Disease]]
* [[Pathway:WP3853|ERK Pathway in Huntington's Disease]]

Revision as of 09:27, 9 February 2021

Explore rare disease pathways on WikiPathways:

Laminopathy pathways

CAKUT (congenital anomalies of the kidney and urinary tract)

Inborn errors of metabolism

Disorders of sex development and fertility

Copy number variation syndromes (CNVs) - duplications or deletions

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