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Aarskog
Agranulocytaire angina
Cockayne
Congenitaal
Cyclisch
De Lange
Door geneesmiddelen geïnduceerd
Dubowitz
Holt-Oram
Infantiele genetische-agranulocytose
Klippel-Trenaunay-Weber
Lienaal
NNO
Nagel-patella
Neutropenie
Neutropenische splenomegalie
Noonan
Periodiek
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Adams
Syndroom van Adams-Stokes
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard
Syndroom van Kostmann
Syndroom van Morgagni
TAR-syndroom
Toxisch
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziekte van Adams-Stokes
Ziekte van Kostmann
Ziekte van Werner-Schultz
Ziektebeeld

Traduction de «Syndroom van Kostmann » (Néerlandais → Anglais) :





syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

Bernard-Horner syndrome


syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

A.-F.syndrome | cystine storage disease


syndroom van Adams | syndroom van Adams-Stokes | syndroom van Morgagni | ziekte van Adams-Stokes

Adams-Stokes disease | Adams-Stokes syndrome | Spens syndrome


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

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


agranulocytaire angina | infantiele genetische-agranulocytose | neutropenie | NNO | neutropenie | congenitaal | neutropenie | cyclisch | neutropenie | door geneesmiddelen geïnduceerd | neutropenie | periodiek | neutropenie | lienaal (primair) | neutropenie | toxisch | neutropenische splenomegalie | ziekte van Kostmann | ziekte van Werner-Schultz

Agranulocytic angina Infantile genetic agranulocytosis Kostmann's disease Neutropenia:NOS | congenital | cyclic | drug-induced | periodic | splenic (primary) | toxic | Neutropenic splenomegaly


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

A rare genetic, poly malformative syndrome with characteristics of progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

Pseudohypoparathyroidism type Ia




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Date index: 2021-09-23
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