Portal:Disease/SpecialIssue
From WikiPathways
(Difference between revisions)
(trying different logo layout) |
Current revision (14:13, 30 January 2019) (view source) |
||
| (4 intermediate revisions not shown.) | |||
| Line 1: | Line 1: | ||
| + | See also the [https://www.wikipathways.org/index.php/Portal:RareDisease Rare disease portal on WikiPathways] | ||
| + | |||
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. | 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. | ||
Rare disease pathways on WikiPathways: | Rare disease pathways on WikiPathways: | ||
| - | [[Image:Rett_Expertise_Centre_logo.jpg| | + | [[Image:EJP RD txt horizontal w.jpg|80px|right]] |
| - | [[Image:Elixir_logo.jpg| | + | [[Image:Rett_Expertise_Centre_logo.jpg|80px|right]] |
| + | [[Image:Elixir_logo.jpg|80px|right]] | ||
* [[:Pathway:WP3584|MECP2 and Associated Rett Syndrome]] | * [[:Pathway:WP3584|MECP2 and Associated Rett Syndrome]] | ||
| - | * [[:Pathway: | + | * [[:Pathway:WP2447|Amyotrophic lateral sclerosis (ALS) SOD1 - CHMP2B MODEL]] |
* [[:Pathway:WP3569|Fanconi Anemia Pathway]] | * [[:Pathway:WP3569|Fanconi Anemia Pathway]] | ||
| + | * [[:Pathway:WP4320|The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome]] | ||
| + | * [[:Pathway:WP4299|Lamin A-processing pathway]] | ||
| + | * [[:Pathway:WP4298|Viral Acute Myocarditis]] | ||
[http://www.orpha.net/consor/cgi-bin/index.php Database for rare diseases (ORPHANET)] | [http://www.orpha.net/consor/cgi-bin/index.php Database for rare diseases (ORPHANET)] | ||
Current revision
See also the Rare disease portal on WikiPathways
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. Rare disease pathways on WikiPathways:
