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Traduzione e analisi delle parole tramite l'intelligenza artificiale ChatGPT
In questa pagina puoi ottenere un'analisi dettagliata di una parola o frase, prodotta utilizzando la migliore tecnologia di intelligenza artificiale fino ad oggi:
- come viene usata la parola
- frequenza di utilizzo
- è usato più spesso nel discorso orale o scritto
- opzioni di traduzione delle parole
- esempi di utilizzo (varie frasi con traduzione)
- etimologia
Cosa (chi) è X disease - definizione
Disease X
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![[[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.
