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Alcoholic hallucinosis
Chronic alcoholism Dipsomania Drug addiction
Delirium tremens
Disorder of personality and behaviour
FRAX
FRAXA syndrome
FXS
Fra-X syndrome
Fragile X syndrome
Fragile x chromosome syndrome
Growth hormone
Hurler-Scheie
Hurler-Scheie syndrome
Insufficiency NOS
Jealousy
MPS I S
Martin-Bell syndrome
Mucopolysaccharidosis type I
Mucopolysaccharidosis type I S
Paranoia
Pituitary hormone
Psychoactive substance abuse
Psychosis NOS
Scheie
Scheie syndrome
Sheehan's syndrome Simmonds' disease
Short stature
Syndrome
Syndrome Hurler

Traduction de «Scheie syndrome » (Anglais → Néerlandais) :

Hurler-Scheie syndrome | mucopolysaccharidosis type I | mucopolysaccharidosis type I H/S | MPS I-H/S [Abbr.]

alfa-L-iduronidase deficiëntie | Hurler/Scheie syndroom | mucopolysaccharidose I




mucopolysaccharidosis type I | mucopolysaccharidosis type I S | Scheie syndrome | MPS I S [Abbr.]

alfa-L-iduronidase deficiëntie | mucopolysaccharidose I-S | Scheie syndroom


Syndrome:Hurler | Hurler-Scheie | Scheie

syndroom van | Hurler | syndroom van | Hurler-Scheie | syndroom van | Scheie


fragile x chromosome syndrome | fragile X syndrome | Fra-X syndrome | FRAXA syndrome | Martin-Bell syndrome | FRAX [Abbr.] | FXS [Abbr.]

fragiel-X-syndroom | FXS [Abbr.]


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 ...[+++]

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.


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

syndroom van Möbius


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

overgeërfde acute myeloïde leukemie


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

dwerggroei van Lorain-Levi | fertiel eunuchoïdisme | geïsoleerde deficiëntie van | ACTH | geïsoleerde deficiëntie van | gonadotropine | geïsoleerde deficiëntie van | groeihormoon | geïsoleerde deficiëntie van | hypofysair hormoon | hypofysaire | cachexie | hypofysaire | insufficiëntie NNO | hypofysaire | kleine gestalte | hypogonadotroop hypogonadisme | idiopathische groeihormoondeficiëntie | necrose van hypofyse (post partum) | panhypopituïtarisme | syndroom van Kallmann | syndroom van Sheehan | ziekte van Simmonds






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Date index: 2024-08-01
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