mutation du gène EGFR

Libellé préféré : mutation du gène EGFR;

Synonyme CISMeF : EGFRm ;

Traductions automatiques des définitions par l'ANS : Un changement dans la séquence des nucléotides du gène EGFR.;

Traductions automatiques par l'ANS : Mutation des gènes HER1; Mutation EGFR; Mutation des gènes EGFR; Mutation des gènes ERBB; Mutation des gènes ERBB1; Mutation du gène du récepteur du facteur croissance épidermique;

Détails

Identifiant d'origine

C98357;

CUI UMLS

C3266992;

Alignements automatiques exacts (par équipe CISMeF)
- EGFR gène mutation [Composé LOINC OBSOLETE ]
- Mutation du gène EGFR [Terme Préféré MedDRA]
- Mutation du gène du récepteur de facteur de croissance épidermique [Terme de bas niveau MedDRA]
Anomalie moléculaire affectant le(s) gène(s)
- gène EGFR [Concept NCIt]
- gène tyrosine kinase réceptrice [Concept NCIt]
Anomalie moléculaire associée à la(aux) pathologie(s)
- gliome diffus de la ligne médiane, EGFR-mutant [Concept NCIt]
Concept appartenant au(x) sous-ensemble(s)
- terminologie CPTAC [Concept NCIt]
- terminologie de CTRP [Concept NCIt]
Correspondances UMLS (même concept)
- Mutation du gène EGFR [Terme Préféré MedDRA]
- Mutation du gène du récepteur de facteur de croissance épidermique [Terme de bas niveau MedDRA]
Est ciblé par
- inhibiteur EGFR ERAS-801 [Concept NCIt]
- zipalertinib [Concept NCIt]
Gène mutant encodant la variation d'une séquence du produit de gène
- EGFR NP_005219.2:p.A750_E758del [Concept NCIt]
- EGFR NP_005219.2:p.A750_K754del [Concept NCIt]
- EGFR NP_005219.2:p.A750_K757del [Concept NCIt]
- EGFR NP_005219.2:p.A763_Y764insFQEA [Concept NCIt]
- EGFR NP_005219.2:p.A767_S768insTLA [Concept NCIt]
- EGFR NP_005219.2:p.C797A [Concept NCIt]
- EGFR NP_005219.2:p.C797S [Concept NCIt]
- EGFR NP_005219.2:p.D761_E762insEAFQ [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insAPW [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insD [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insDG [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insG [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insGD [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insGL [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insGT [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insGV [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insMATP [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insN [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insNPH [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insSVD [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insSVP [Concept NCIt]
- EGFR NP_005219.2:p.D770_N771insSVQ [Concept NCIt]
- EGFR NP_005219.2:p.D770fs*61 [Concept NCIt]
- EGFR NP_005219.2:p.E709* [Concept NCIt]
- EGFR NP_005219.2:p.E746_A750del [Concept NCIt]
- EGFR NP_005219.2:p.E746_E749del [Concept NCIt]
- EGFR NP_005219.2:p.E746_P753del [Concept NCIt]
- EGFR NP_005219.2:p.E746_R748del [Concept NCIt]
- EGFR NP_005219.2:p.E746_S752del [Concept NCIt]
- EGFR NP_005219.2:p.E746_T751del [Concept NCIt]
- EGFR NP_005219.2:p.E746del [Concept NCIt]
- EGFR NP_005219.2:p.G719A [Concept NCIt]
- EGFR NP_005219.2:p.G719C [Concept NCIt]
- EGFR NP_005219.2:p.G719D [Concept NCIt]
- EGFR NP_005219.2:p.G719S [Concept NCIt]
- EGFR NP_005219.2:p.G719V [Concept NCIt]
- EGFR NP_005219.2:p.G719X [Concept NCIt]
- EGFR NP_005219.2:p.G719fs*29 [Concept NCIt]
- EGFR NP_005219.2:p.G796R [Concept NCIt]
- EGFR NP_005219.2:p.G796S [Concept NCIt]
- EGFR NP_005219.2:p.G796X [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insAH [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insG [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insGH [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insGNPH [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insH [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insNPH [Concept NCIt]
- EGFR NP_005219.2:p.H773_V774insPH [Concept NCIt]
- EGFR NP_005219.2:p.I740_P741insPVAIKI [Concept NCIt]
- EGFR NP_005219.2:p.I744_K745insKIPVAI [Concept NCIt]
- EGFR NP_005219.2:p.I789_L792del [Concept NCIt]
- EGFR NP_005219.2:p.K29_N298insG [Concept NCIt]
- EGFR NP_005219.2:p.K745_A750del [Concept NCIt]
- EGFR NP_005219.2:p.K745_E746insVPVAIK [Concept NCIt]
- EGFR NP_005219.2:p.K745_E749del [Concept NCIt]
- EGFR NP_005219.2:p.K745_L747del [Concept NCIt]
- EGFR NP_005219.2:p.L718Q [Concept NCIt]
- EGFR NP_005219.2:p.L718V [Concept NCIt]
- EGFR NP_005219.2:p.L718X [Concept NCIt]
- EGFR NP_005219.2:p.L747_A750del [Concept NCIt]
- EGFR NP_005219.2:p.L747_A755del [Concept NCIt]
- EGFR NP_005219.2:p.L747_E749del [Concept NCIt]
- EGFR NP_005219.2:p.L747_K754del [Concept NCIt]
- EGFR NP_005219.2:p.L747_P753del [Concept NCIt]
- EGFR NP_005219.2:p.L747_S752del [Concept NCIt]
- EGFR NP_005219.2:p.L747_T751del [Concept NCIt]
- EGFR NP_005219.2:p.L747del [Concept NCIt]
- EGFR NP_005219.2:p.L792F [Concept NCIt]
- EGFR NP_005219.2:p.L792H [Concept NCIt]
- EGFR NP_005219.2:p.L792X [Concept NCIt]
- EGFR NP_005219.2:p.L792Y [Concept NCIt]
- EGFR NP_005219.2:p.L858A [Concept NCIt]
- EGFR NP_005219.2:p.L858G [Concept NCIt]
- EGFR NP_005219.2:p.L858K [Concept NCIt]
- EGFR NP_005219.2:p.L858M [Concept NCIt]
- EGFR NP_005219.2:p.L858P [Concept NCIt]
- EGFR NP_005219.2:p.L858Q [Concept NCIt]
- EGFR NP_005219.2:p.L858W [Concept NCIt]
- EGFR NP_005219.2:p.L861F [Concept NCIt]
- EGFR NP_005219.2:p.L861P [Concept NCIt]
- EGFR NP_005219.2:p.L861Q [Concept NCIt]
- EGFR NP_005219.2:p.L861R [Concept NCIt]
- EGFR NP_005219.2:p.L861V [Concept NCIt]
- EGFR NP_005219.2:p.M766_A767insAI [Concept NCIt]
- EGFR NP_005219.2:p.M766_A767insASV [Concept NCIt]
- EGFR NP_005219.2:p.N756_L760del [Concept NCIt]
- EGFR NP_005219.2:p.N771_P772insH [Concept NCIt]
- EGFR NP_005219.2:p.N771_P772insN [Concept NCIt]
- EGFR NP_005219.2:p.P753_I759del [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insDHP [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insDNP [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insNP [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insNPH [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insPR [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insQV [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insTHP [Concept NCIt]
- EGFR NP_005219.2:p.P772_H773insYNP [Concept NCIt]
- EGFR NP_005219.2:p.P772_V774insPHV [Concept NCIt]
- EGFR NP_005219.2:p.R748_P753del [Concept NCIt]
- EGFR NP_005219.2:p.R748_S752del [Concept NCIt]
- EGFR NP_005219.2:p.S492R [Concept NCIt]
- EGFR NP_005219.2:p.S752_I759del [Concept NCIt]
- EGFR NP_005219.2:p.S752_V769del [Concept NCIt]
- EGFR NP_005219.2:p.S768I [Concept NCIt]
- EGFR NP_005219.2:p.S768_V769insAWT [Concept NCIt]
- EGFR NP_005219.2:p.S768_V769insVAS [Concept NCIt]
- EGFR NP_005219.2:p.T751_E758del [Concept NCIt]
- EGFR NP_005219.2:p.V765_M766insMAS [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insASV [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insCV [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insDNV [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insGSV [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insGV [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insGVV [Concept NCIt]
- EGFR NP_005219.2:p.V769_D770insMASVD [Concept NCIt]
- EGFR NP_005219.2:p.V774_C775insHV [Concept NCIt]
- EGFR NP_005219.2:p.V774del [Concept NCIt]
- EGFR NP_005219.2:p.V834del [Concept NCIt]
- EGFR NP_005219.2:p.Y764_V765insHH [Concept NCIt]
- EGFR T790M [Concept NCIt]
- mutation par substitution de l’exon 21 de l'EGFR (L858R) [Concept NCIt]
- variant de la protéine EGFR [Concept NCIt]
Type(s) sémantique(s)
- dysfonctionnement cellulaire ou moléculaire [Type sémantique UMLS]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

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