Portal:RareDisease/Intro

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Current revision (12:11, 26 November 2020) (view source)
 
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This portal is funded by:
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This portal highlights WikiPathways content related to rare genetic human diseases, and is designed
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as a central organizing point for exploring, curating and expanding the collection of rare disease pathways. [[Image:Wordcloud2.png|400px|Image: 400 pixels|right|Image on right]]
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[[Image:LogoEJPRD1.png|100px|Image: 100 pixels]]
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A rare or orphan disease is a disease which affects relatively few people. The exact definition varies <br />
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between 1:1000 and 1:200.000. E.g. it can be 1:1500 (USA) , 1:2000 (EU) or 1:2500 (Japan). Rare diseases <br />
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are mostly caused by genetic variation making them chronic and hard to cure. The severity depends on <br />
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the affected gene and its physiological implications.
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This portal is also featured in the latest [https://doi.org/10.1093/nar/gkaa1024 NAR Database Issue on WikiPathways].
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This portal is funded by:
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[[Image:EJP_RD_txt_horizontal_w.jpg|300px|Image: 300 pixels|left|Image on left]]
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[[Image:Elixir_logo.jpg|100px|Image: 100 pixels‎|left|Image on left]]
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[[Image:Rett_Expertise_Centre_logo.jpg‎‎|100px|Image: 100 pixels|Image: 100 pixels‎|left|Image on left]]

Current revision

This portal highlights WikiPathways content related to rare genetic human diseases, and is designed

as a central organizing point for exploring, curating and expanding the collection of rare disease pathways.
Image on right

A rare or orphan disease is a disease which affects relatively few people. The exact definition varies
between 1:1000 and 1:200.000. E.g. it can be 1:1500 (USA) , 1:2000 (EU) or 1:2500 (Japan). Rare diseases
are mostly caused by genetic variation making them chronic and hard to cure. The severity depends on
the affected gene and its physiological implications.

This portal is also featured in the latest NAR Database Issue on WikiPathways.

This portal is funded by:

Image on left
Image on left
Image on left
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