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Combined immunodeficiency (severe), X-linked
IL2RG
T-B+ severe combined immunodeficiency due to gamma chain deficiency
Centrum Menselijke Erfelijkheid - KUL
Hemophilia A
F8
Hemophilia A
,
Severe hemophilia A
,
Moderate hemophilia A
,
Mild hemophilia A
,
Bleeding disorder in hemophilia A carriers
Centre de Génétique Médicale UCL
Hemophilia A
F8
Hemophilia A
,
Mild hemophilia A
,
Severe hemophilia A
,
Moderate hemophilia A
,
Bleeding disorder in hemophilia A carriers
Centrum Menselijke Erfelijkheid - KUL
Sessile serrated polyposis syndrome (RNF43 gene)
RNF43
Serrated polyposis syndrome
Centre de Génétique Humaine - CHU Sart-Tilman
Glycogen storage disease type 9
PHKA2
Glycogen storage disease due to liver phosphorylase kinase deficiency
Centre de Génétique Humaine - CHU Sart-Tilman
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