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Abt-Letterer-Siwe disease
Abt-Letterer-Siwe syndrome
Acute disseminated histiocytosis X
Alcoholic hallucinosis
Chronic alcoholism Dipsomania Drug addiction
DAF syndrome
Delirium tremens
Disorder of personality and behaviour
Histiocytosis X
Histiocytosis X syndrome
Infectious reticulo-endotheliosis
Jealousy
LCH
Langerhans cell histiocytosis
Langerhans' cell granulomatosis
Letterer-Siwe disease
Lipid histiocytosis
Lipoid histiocytosis
Multifocal multisystem Langerhans cell histiocytosis
Niemann-Pick disease
Other histiocytosis syndromes
Paranoia
Psychoactive substance abuse
Psychosis NOS
Sphingomyelin lipidosis
Sphingomyelinase deficiency

Traduction de «other histiocytosis syndromes » (Anglais → Néerlandais) :

Other histiocytosis syndromes

overige histiocytosesyndromen


histiocytosis X | histiocytosis X syndrome | Langerhans' cell granulomatosis | Langerhans cell histiocytosis | LCH [Abbr.]

histiocytose-X | Langerhans Cel Histiocytose | LHC [Abbr.]


Abt-Letterer-Siwe disease | Abt-Letterer-Siwe syndrome | acute disseminated histiocytosis X | infectious reticulo-endotheliosis | Letterer-Siwe disease | multifocal multisystem Langerhans cell histiocytosis

syndroom van Abt-Siwe-Letterer


DAF syndrome | lipid histiocytosis | lipoid histiocytosis (classical phosphatide) | Niemann-Pick disease | sphingomyelin lipidosis | sphingomyelinase deficiency

ziekte van Niemann-Pick


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 flui ...[+++]

Omschrijving: Dit blok omvat een grote verscheidenheid van stoornissen van verschillende ernst en klinische vorm, die evenwel alle aan het gebruik van een of meer psychoactieve middelen, al dan niet op medisch voorschrift, zijn toe te schrijven. De betrokken stof wordt aangegeven door middel van het derde teken van de code en het vierde teken specificeert de klinische toestand; deze codering dient, waar nodig, gebruikt te worden voor elk gespecificeerd middel, met dien verstande dat niet elk vierde teken van toepassing is op elke stof.


Definition: A heterogeneous group of disorders that share the characteristic of an onset in childhood but otherwise differ in many respects. Some of the conditions represent well-defined syndromes but others are no more than symptom complexes that need inclusion because of their frequency and association with psychosocial problems, and because they cannot be incorporated into other syndromes.

Omschrijving: Een heterogene groep stoornissen die een kenmerkend begin op kinderleeftijd gemeen hebben, maar overigens in vele opzichten van elkaar verschillen. Sommige van deze toestanden vertegenwoordigen goed gedefinieerde syndromen, maar andere zijn niet meer dan symptomencomplexen die genoemd moeten worden wegens hun veelvuldig voorkomen en samengaan met psychosociale stoornis en omdat ze niet bij andere syndromen kunnen worden ondergebracht.


Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may

multiple sclerose, ichthyosis, factor VIII-deficiëntiesyndroom


Syndrome with characteristics of precocious puberty (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa

spastische paraplegie, vroegtijdige puberteit


A rare syndromic microphthalmia disorder with characteristics of microphthalmia with coloboma (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali

X-gebonden colobomateuze microftalmie, microcefalie, intellectuele achterstand, kleine gestalte-syndroom


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