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Adair Dighton syndrome
Alcoholic hallucinosis
Bartter syndrome
Bartter syndrome type 3
Bartter syndrome type 4
Bartter syndrome type 4a
Bartter's syndrome
Blegvad-Haxthausen syndrome
Brittle bone disease
Brittle bone syndrome
Chronic alcoholism Dipsomania Drug addiction
Delirium tremens
Disorder of personality and behaviour
Glass bone disease
Jealousy
Lobstein disease
Lobstein’s disease
Morquio
Osteogenesis imperfecta
Osteogenesis imperfecta tarda
Osteogenesis imperfecta type I
Paranoia
Psychoactive substance abuse
Psychosis NOS
Sanfilippo
Schwartz-Bartter syndrome

Traduction de «bartter syndrome type » (Anglais → Néerlandais) :





Bartter syndrome type 4

antenataal Bartter-syndroom type 4






Adair Dighton syndrome | Blegvad-Haxthausen syndrome | brittle bone disease | brittle bone syndrome | glass bone disease | Lobstein disease | Lobstein’s disease | osteogenesis imperfecta | osteogenesis imperfecta tarda | osteogenesis imperfecta type I

osteogenesis imperfecta tarda | osteogenesis imperfecta type I


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 ...[+++]

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.




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

bèta-glucuronidasedeficiëntie | mucopolysaccharidose, type III, IV, VI, VII | syndroom (van) | Maroteaux-Lamy (licht)(ernstig) | syndroom (van) | Morquio(-achtig)(klassiek) | syndroom (van) | Sanfilippo (type B)(type C)(type D)


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