Portal:RareDisease/News

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* [[Pathway:WP4656|Joubert Syndrome]]
* [[Pathway:WP4656|Joubert Syndrome]]
* [[Pathway:WP4535|Envelope proteins and their potential roles in EDMD physiopathology]]
* [[Pathway:WP4535|Envelope proteins and their potential roles in EDMD physiopathology]]
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* [[Pathway:WP4803|Ciliopathies]]
 +
 +
Laminopathy pathways
* [[Pathway:WP4299|Lamin A-processing pathway]]
* [[Pathway:WP4299|Lamin A-processing pathway]]
* [[Pathway:WP4320|The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome]]
* [[Pathway:WP4320|The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome]]
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* [[Pathway:WP4657|22q11.2 Deletion Syndrome]]
* [[Pathway:WP4657|22q11.2 Deletion 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]]

Revision as of 13:51, 22 June 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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