Voer een woord of zin in in een taal naar keuze 👆
Taal:
Vertaling en analyse van woorden door kunstmatige intelligentie ChatGPT
Op deze pagina kunt u een gedetailleerde analyse krijgen van een woord of zin, geproduceerd met behulp van de beste kunstmatige intelligentietechnologie tot nu toe:
- hoe het woord wordt gebruikt
- gebruiksfrequentie
- het wordt vaker gebruikt in mondelinge of schriftelijke toespraken
- opties voor woordvertaling
- Gebruiksvoorbeelden (meerdere zinnen met vertaling)
- etymologie
Wat (wie) is X disease - definitie
Disease X
.jpg?width=200)
![[[Jeremy Farrar]], Chair of the WHO R&D Blueprint Scientific Advisory Group<ref name=WHO5/>](https://commons.wikimedia.org/wiki/Special:FilePath/Jeremy Farrar C0058569 Wellcome Images.jpg?width=200 "[[Jeremy Farrar]], Chair of the WHO R&D Blueprint Scientific Advisory Group<ref name=WHO5/>")
PLACEHOLDER NAME THAT WAS ADOPTED BY THE WORLD HEALTH ORGANIZATION (WHO) IN FEBRUARY 2018 ON A SHORTLIST OF BLUEPRINT PRIORITY DISEASES TO REPRESENT A HYPOTHETICAL, UNKNOWN PATHOGEN THAT COULD CAUSE A FUTURE EPIDEMIC
Blueprint priority list; Blueprint priority disease; Pathogen X; R&D Blueprint
Disease X is a placeholder name that was adopted by the World Health Organization (WHO) in February 2018 on their shortlist of blueprint priority diseases to represent a hypothetical, unknown pathogen that could cause a future epidemic. The WHO adopted the placeholder name to ensure that their planning was sufficiently flexible to adapt to an unknown pathogen (e.
X-linked lymphoproliferative disease
LYMPHOPROLIFERATIVE DISORDER
Duncan's disease; X-linked lymphoproliferative syndrome; Purtilo syndrome; XLP (hematology)
X-linked lymphoproliferative disease (also known as Duncan disease or Purtilo syndrome and abbreviated as XLP) is a lymphoproliferative disorder, usually caused by SH2DIA gene mutations in males. XLP-positive individuals experience immune system deficiencies that render them unable to effectively respond to the Epstein-Barr virus (EBV), a common virus in humans that typically induces mild symptoms or infectious mononucleosis (IM) in patients.
X-linked Charcot-Marie-Tooth disease
CHARCOT-MARIE-TOOTH DISEASE THAT HAS MATERIAL BASIS IN X-LINKED INHERITANCE OF A POINT MUTATION IN THE CONNEXIN-32 GENE
Draft:X-linked Charcot-Marie-Tooth disease; X-linked Charcot-Marie-Tooth disease
X-linked Charcot-Marie-Tooth disease is a group of genetic disorders and a type of Charcot-Marie-Tooth disease characterized by sensory loss associated with muscle weakness and atrophy alongside many other symptoms.
