Portal:RareDisease/News

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* [[Pathway:WP4905|1q21.1 copy number variation syndrome]]
* [[Pathway:WP4905|1q21.1 copy number variation syndrome]]
* [[Pathway:WP4906|3q29 copy number variation syndrome]]
* [[Pathway:WP4906|3q29 copy number variation syndrome]]
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* [[Pathway:WP4657|22q11.2 Deletion Syndrome]]
+
* [[Pathway:WP4657|22q11.2 copy number variation syndrome]]
* [[Pathway:WP3998|Prader-Willi and Angelman Syndrome]]
* [[Pathway:WP3998|Prader-Willi and Angelman Syndrome]]
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* [[Pathway:WP4932|Williams Beuren region duplication syndrome]]
+
* [[Pathway:WP4932|7q11.23 copy number variation syndrome]]
* [[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:WP4950|16p11.2 distal deletion syndrome]]
* [[Pathway:WP4949|16p11.2 proximal deletion syndrome]]
* [[Pathway:WP4949|16p11.2 proximal deletion syndrome]]

Revision as of 08:35, 18 September 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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