Portal:RareDisease/News

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(Explore rare disease pathways on WikiPathways:)
(Explore rare disease pathways on WikiPathways:)
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* [[Pathway:WP4656|Joubert Syndrome]]
* [[Pathway:WP4656|Joubert Syndrome]]
* [[Pathway:WP4844|The influence of laminopathies on Wnt signaling]]
* [[Pathway:WP4844|The influence of laminopathies on Wnt signaling]]
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* [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]]
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* [[Pathway:WP4879|Interacting Laminopathic Pathways]]
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* [[Pathway:WP4830|GDNF/RET signalling axis]]
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Renal diseases and congenital malformations
* [[Pathway:WP4818|Conversion of Angiotensinogen to Angiotensin II]]
* [[Pathway:WP4818|Conversion of Angiotensinogen to Angiotensin II]]
* [[Pathway:WP4823|Genes controlling renal nephrogenesis]]
* [[Pathway:WP4823|Genes controlling renal nephrogenesis]]
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* [[Pathway:WP4879|Interacting Laminopathic Pathways]]
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* [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]]
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* [[Pathway:WP4830|GDNF/RET signalling axis]]
Inborn errors of metabolism
Inborn errors of metabolism

Revision as of 15:12, 30 April 2020

Explore rare disease pathways on WikiPathways:

Renal diseases and congenital malformations

Inborn errors of metabolism

Disorders of sex development and fertility

Copy number variation syndromes (CNVs) - duplications or deletions

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