Portal:RareDisease/News

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CAKUT (congenital anomalies of the kidney and urinary tract)
CAKUT (congenital anomalies of the kidney and urinary tract)
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* [[Pathway:WP4818|Conversion of Angiotensinogen to Angiotensin II]]
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* [[Pathway:WP5053|Development of uretric collection system]]
* [[Pathway:WP4823|Genes controlling renal nephrogenesis]]
* [[Pathway:WP4823|Genes controlling renal nephrogenesis]]
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* [[Pathway:WP4838|Regucalcin in proximal tubule epithelial kidney cells]]
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* [[Pathway:WP5052|Nephrogenesis]]
* [[Pathway:WP4830|GDNF/RET signalling axis]]
* [[Pathway:WP4830|GDNF/RET signalling axis]]

Revision as of 09:13, 8 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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