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Aarskog
Autosomaal recessief hyperimmunoglobuline M-syndroom
Cockayne
De Lange
Dubowitz
Holt-Oram
Hyper-IgE-syndroom
Hyperimmunoglobuline E-syndroom
Klippel-Trenaunay-Weber
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
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 Morgagni
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziekte van Adams-Stokes

Vertaling van "Hyperimmunoglobuline E-syndroom " (Nederlands → Engels) :

hyperimmunoglobuline E-syndroom [hyper-IgE-syndroom]

Hyperimmunoglobulin E [IgE] syndrome


autosomaal recessief hyperimmunoglobuline M-syndroom

Autosomal recessive hyper-IgM syndrome


hyperimmunoglobuline M-syndroom met gevoeligheid voor opportunistische infectie

A rare genetic non-severe combined immunodeficiency disorder with characteristics of normal or elevated IgM serum levels with low or absent IgG, IgA and IgE serum concentrations, which manifests with recurrent or severe bacterial infections and incre


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 Bernard | syndroom van Horner | syndroom van Horner-Bernard

Bernard-Horner 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


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


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

Pseudohypoparathyroidism type Ia




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'Hyperimmunoglobuline E-syndroom' ->

Date index: 2022-01-24
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