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Alcoholic hallucinosis
Angioma capillare et venosum calcificans
Angiomatosis meningo-oculofacialis
Bardet-Biedl syndrome
Biedl's syndrome
Biemond's syndrome
CS
Chronic alcoholism Dipsomania Drug addiction
Cockayne
Cockayne disease
Cockayne syndrome
Congenital neuroectodermal dysplasia
Cutaneocerebral angioma
De Lange
Delirium tremens
Dimitri-disease
Disorder of personality and behaviour
Dubowitz
Encephalotrigeminal angiomatosis
Encephalotrigeminal syndrome
Growth hormone
Insufficiency NOS
Jealousy
Kalischer's syndrome
Krabbe's II syndrome
Laurence-Moon-Biedl syndrome
Moon-Bardet-Biedl syndrome
Neurocutaneous syndrome
Noonan
Paranoia
Parkes Weber's syndrome
Pituitary hormone
Prader-Willi
Psychoactive substance abuse
Psychosis NOS
Robinow-Silverman-Smith
Russell-Silver
Seckel
Sheehan's syndrome Simmonds' disease
Short stature
Smith-Lemli-Opitz
Sturge's disease
Sturge's syndrome
Sturge-Kalischer-Weber syndrome
Sturge-Weber disease
Sturge-Weber syndrome
Sturge-Weber-Dimitri syndrome
Syndrome Aarskog
Weber-Dimitri syndrome
Xeroderma pigmentosum and Cockayne syndrome complex

Traduction de «cockayne syndrome » (Anglais → Français) :



Cockayne disease | Cockayne syndrome

nanisme hérédo-familial polydystrophique | syndrome de Cockayne


Xeroderma pigmentosum and Cockayne syndrome complex

complexe Xeroderma pigmentosum-syndrome de Cockayne


Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz

Syndrome de:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome

syndrome de Sturge-Weber | angiomatose encéphalotrigéminée de Sturge-Weber-Krabbe | angiomatose méningo-oculo-faciale | angiomatose neuro-cutanée | angiomatose neuro-oculo-cutanée | maladie de Sturge-Weber-Krabbe | neuro-ectodermo-dysplasie congénitale | syndrome de Brushfield-Wyatt | syndrome neuro-cutané | syndrome de Parkes-Weber | syndrome de Sturge-Weber-Krabbe | syndrome de Weber-Dimitri


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


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 sel ...[+++]

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, ...[+++]


A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib

syndrome de Mœbius


A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c

leucémie aigüe myéloïde héréditaire


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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