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Alcoholic hallucinosis
Basal cell naevus syndrome
Basal cell nevus syndrome
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
Gorlin syndrome
Gorlin-Goltz syndrome
Growth hormone
Haas
Head of humerus
Insufficiency NOS
Jealousy
Martin-Bell syndrome
Osteochondrosis
Panner
Panner disease
Panner syndrome
Panner's disease
Paranoia
Pituitary hormone
Psychoactive substance abuse
Psychosis NOS
Sheehan's syndrome Simmonds' disease
Short stature
Syndrome

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





Osteochondrosis (juvenile) of:capitulum of humerus [Panner] | head of humerus [Haas] |

osteochondrose (juveniel) van | capitulum humeri [Panner] | osteochondrose (juveniel) van | caput humeri [Haas]


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

fragiel-X-syndroom | FXS [Abbr.]


basal cell naevus syndrome | basal cell nevus syndrome | Gorlin syndrome | Gorlin-Goltz syndrome

basocellulair naevussyndroom


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.


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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