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Aarskog
Artropathie
Cockayne
De Lange
Dubowitz
Febris uveo-parotidea
Febris uveoparotidea
Heerfordt
Holt-Oram
Iridocyclitis
Klippel-Trenaunay-Weber
LBWC
Myocarditis
Myositis
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Heerfordt
Syndroom van Horner
Syndroom van Horner-Bernard
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziektebeeld

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

febris uveo-parotidea | syndroom van Heerfordt

Heerfordt's disease | Heerfordt's syndrome




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


artropathie (M14.8)bij sarcoïdose | iridocyclitis (H22.1)bij sarcoïdose | myocarditis (I41.8)bij sarcoïdose | myositis (M63.3)bij sarcoïdose | multipele verlammingen van hersenzenuwen (G53.2)bij sarcoïdose | febris uveoparotidea [Heerfordt]

Iridocyclitis in sarcoidosis+ (H22.1*) Multiple cranial nerve palsies in sarcoidosis+ (G53.2*) Sarcoid:arthropathy+ (M14.8*) | myocarditis+ (I41.8*) | myositis+ (M63.3*) | Uveoparotid fever [Heerfordt]


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


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


LBWC (limb body wall complex)-syndroom

Limb body wall complex


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: 2023-04-16
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