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Alcoholic hallucinosis
Chronic alcoholism Dipsomania Drug addiction
Clinically compatible cases
Clinically compatible defect
Clinically compatible symptom
Delirium tremens
Disorder of personality and behaviour
Jealousy
Paranoia
Psychoactive substance abuse
Psychosis NOS

Vertaling van "clinically compatible defect " (Engels → Frans) :

clinically compatible defect

anomalie clinique compatible


clinically compatible symptom

symptôme clinique compatible


clinically compatible cases

cas compatibles sur le plan clinique


Definition: This block contains a wide variety of disorders that differ in severity and clinical form but that are all attributable to the use of one or more psychoactive substances, which may or may not have been medically prescribed. The third character of the code identifies the substance involved, and the fourth character specifies the clinical state. The codes should be used, as required, for each substance specified, but it should be noted that not all fourth character codes are applicable to all substances. Identification of the psychoactive substance should be based on as many sources of information as ...[+++]

Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les rubriques F10-F19: Code Titre .0 Intoxication aiguë Etat consécutif à la prise d'une substance psycho-active et entraînant des perturbations de la conscience, des facultés cognitives, de la perception, de l'affect ou du comportement, ou d'autres fonctions et réponses psychophysiologiques. Les perturbations sont directement liées aux effets pharmacologiques aigus de la substance consommée, et disparaissent avec le temps, avec guérison complète, sauf dans les cas ayant entraîné des lésions organiques ou d'autres ...[+++]


A rare genetic non-syndromic developmental defect of the eye disorder with the association of posterior microphthalmia, retinal dystrophy compatible with retinitis pigmentosa, localised foveal schisis and optic disc drusen. Patients present high hype

syndrome de microphtalmie-rétinite pigmentaire-fovéoschisis-drusen de la papille optique


A recently described syndrome associated with variable clinical features including behavioral abnormalities, developmental delay, congenital heart defects and skeletal anomalies. This syndrome is caused by interstitial duplications encompassing 16p13

syndrome de microduplication 16p13.11


A rare genetic disorder of metabolite absorption or transport with characteristics of persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical findings consistent with a

déficit maternel en riboflavine




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Date index: 2025-10-08
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