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Alcoholic hallucinosis
Biemond syndrome type 2
Chronic alcoholism Dipsomania Drug addiction
Delirium tremens
Disease Charcot-Marie-Tooth
Disorder of personality and behaviour
Déjerine-Sottas
Extracapillary glomerulonephritis
Fatigue syndrome
Focal and segmental hyalinosis
Focal glomerulonephritis
Jealousy
Minimal change lesion
Morquio
Paranoia
Proliferative glomerulonephritis NOS
Psychoactive substance abuse
Psychosis NOS
Sanfilippo
Sclerosis

Translation of "Biemond syndrome type 2 " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Biemond syndrome type 2

syndrome de Biemond type 2
SNOMEDCT-BE (disorder) / 717887003
SNOMEDCT-BE (disorder) / 717887003


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 possible. These include self-report data, analysis of blood and other body fluids, characteristic physical and psychological symptom ...[+++]

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 complications. Parmi les complications, on peut citer: les traumatismes, les fausses routes avec inhalation de vomissements, le delirium, ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F10-F19
WORLD HEALTH ORGANIZATION ICD-10: F10-F19


Modifiers The following fourth-character subdivisions classify morphological changes and are for use with categories N00-N07. Subdivisions .0-.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three-character categories relate to clinical syndromes. Code Title .0 Minor glomerular abnormality Minimal change lesion .1 Focal and segmental glomerular lesions Focal and segmental:hyalinosis | sclerosis | Focal glomerulonephritis .2 Diffuse membranous glomerulonephritis .3 Diffuse mesangial proliferative glomerulonephritis .4 Diffuse endocapillary proliferative glomerulonephritis ...[+++]

Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les catégories N00-N07 pour classer les modifications morphologiques. Les subdivisions .0-.8 ne doivent être normalement utilisées que s'il y a eu identification précise (par biopsie rénale ou autopsie). Les catégories à trois caractères concernent les syndromes cliniques. Code Titre .0 Anomalies glomérulaires mineures Lésions minimes .1 Lésions glomérulaires segmentaires et focales Glomérulonéphrite focale Hyalinose | Sclérose | segmentaire et focale | .2 Glomérulonéphrite membraneuse diffuse .3 Glomérulonéphrite proliférative mésangiale diffuse ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: N00-N08
WORLD HEALTH ORGANIZATION ICD-10: N00-N08


Definition: Considerable cultural variations occur in the presentation of this disorder, and two main types occur, with substantial overlap. In one type, the main feature is a complaint of increased fatigue after mental effort, often associated with some decrease in occupational performance or coping efficiency in daily tasks. The mental fatiguability is typically described as an unpleasant intrusion of distracting associations or recollections, difficulty in concentrating, and generally inefficient thinking. In the other type, the emphasis is on feelings of bodily or physical weakness and exhaustion after only minimal effort, accompanie ...[+++]

Définition: Il existe des variations culturelles importantes dans les manifestations de ce trouble, qui comporte deux types essentiels, ayant de nombreux points communs. Dans le premier type, la caractéristique essentielle est une plainte concernant une fatigue accrue après des efforts mentaux, souvent associée à une certaine diminution des performances professionnelles et des capacités à faire face aux tâches quotidiennes. La fatigabilité mentale est décrite typiquement comme une distractibilité due à une intrusion désagréable d'associations et de souvenirs, une difficulté de concentration ou une pensée globalement inefficace. Dans le d ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F48.0
WORLD HEALTH ORGANIZATION ICD-10: F48.0


Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)

Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)
WORLD HEALTH ORGANIZATION ICD-10: E76.2
WORLD HEALTH ORGANIZATION ICD-10: E76.2


Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome

Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0


A rare genetic syndromic intellectual disability characterized by mild intellectual disability, short stature with high body mass index, short neck with cervical gibbus and dysmorphic facial features. A metabolic syndrome, including type 2 diabetes,

syndrome de microdélétion 9 q31.1q31.3
SNOMEDCT-BE (disorder) / 773493002
SNOMEDCT-BE (disorder) / 773493002


This syndrome has characteristics of Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two mater

syndrome de maladie de Hirschsprung-brachydactylie type D
SNOMEDCT-BE (type D brachydactyly). It has been described in four males from one family (two brothers and two mater / 721222007
SNOMEDCT-BE (disorder) / 721222007


A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects

syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004


A rare genetic syndromic intellectual disability characterised by mild intellectual disability, short stature with high body mass index, short neck with cervical gibbus and dysmorphic facial features. A metabolic syndrome, including type 2 diabetes,

del(9)(q31.1q31.3)
SNOMEDCT-BE (disorder) / 773493002
SNOMEDCT-BE (disorder) / 773493002
IN-CONTEXT TRANSLATIONS


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'Biemond syndrome type 2'

Date index:2021-09-17 -

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