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Alcoholic hallucinosis
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Bardet-Biedl syndrome
Biedl's syndrome
Biemond's syndrome
Blue sclera syndrome
Brancher deficiency
Brancher enzyme deficiency
Chronic alcoholism Dipsomania Drug addiction
Congenital nonhaemolytic jaundice with kernicterus
Congenital nonhemolytic jaundice with kernicterus
Crigler-Najjar disease
Crigler-Najjar syndrome
Crigler-Najjar syndrome type II
Delirium tremens
Disorder of personality and behaviour
Eddowes'syndrome
Eddowes-Spurway syndrome
Familia
GSD IV
Glycogen storage disease type IV
Glycogenosis IV
Growth hormone
Insufficiency NOS
Jealousy
Laurence-Moon-Biedl syndrome
Lobstein's syndrome
Moon-Bardet-Biedl syndrome
Najjar syndrome
Najjar-Andersen syndrome
Paranoia
Pituitary hormone
Psychoactive substance abuse
Psychosis NOS
Sheehan's syndrome Simmonds' disease
Short stature
Spurway's syndrome

Übersetzung für "Najjar syndrome " (Englisch → Französisch) :





Crigler-Najjar syndrome type II

syndrome de Crigler-Najjar type 2




congenital nonhaemolytic jaundice with kernicterus | congenital nonhemolytic jaundice with kernicterus | Crigler-Najjar disease | Crigler-Najjar syndrome

hyperbilirubinémie idiopathique | ictère congénital non hémolytique | ictère congénital non hémolytique avec ictère nucléaire de Crigler-Najjar | ictère familial congénital de Crigler-Najjar | ictère nucléaire de Crigler et Najjar | maladie de Crigler-Najjar | syndrome de Crigler-Najjar


Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]

maladie d'Andersen [ glycogénose musculaire type IV ]


Bardet-Biedl syndrome | Biedl's syndrome | Biemond's syndrome | Laurence-Moon-Biedl syndrome | Moon-Bardet-Biedl syndrome

syndrome de Laurence-Biedl | syndrome de Laurence-Moon-Bardet


blue sclera syndrome | Eddowes-Spurway syndrome | Eddowes'syndrome | Lobstein's syndrome | Spurway's syndrome

syndrome d'Eddowes


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, ...[+++]


Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of:gonadotropin | growth hormone | pituitary hormone | Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary:cachexia | insufficiency NOS | short stature | Sheehan's syndrome Simmonds' disease

Cachexie hypophysaire Hypogonadisme hypogonadotrophique Insuffisance (de):hormone de croissance idiopathique | isolée en:gonadotrophine | hormone de croissance | hormone hypophysaire | staturale pituitaire SAI | Maladie de Simmonds Nécrose pituitaire (post-partum) Panhypopituitarisme Syndrome de:eunuchoïdisme fertile | Kallmann | Lorain-Lévi | Sheehan


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