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Fabry disease: Difference between revisions
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Fabry disease is a genetic condition involving lysosomal storage (E75.2)<ref>https://de.wikipedia.org/wiki/Morbus_Fabry</ref> | Fabry disease is a genetic condition involving lysosomal storage (E75.2)<ref>https://de.wikipedia.org/wiki/Morbus_Fabry</ref> | ||
<gallery> | <gallery>File:Morbus Fabry affected organs.svg.png</gallery> | ||
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https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/UCM616598.htm | https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/UCM616598.htm | ||
<references/> | <references/> | ||
Revision as of 00:35, 11 August 2018
Fabry disease is a genetic condition involving lysosomal storage (E75.2)[1]
https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/UCM616598.htm