Portal:RareDisease/News

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* [[Pathway:WP4940|15q11.2 copy number variation syndrome]]
* [[Pathway:WP4940|15q11.2 copy number variation syndrome]]
* [[Pathway:WP4942|15q13.3 copy number variation syndrome]]
* [[Pathway:WP4942|15q13.3 copy number variation syndrome]]
 +
* [[Pathway:WP4950|16p11.2 distal deletion syndrome]]
 +
* [[Pathway:WP4949|16p11.2 proximal deletion syndrome]]

Revision as of 08:56, 28 July 2020

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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