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ACTH-independent macronodular adrenal hyperplasia 2 / Cushing syndrome
ARMC5
Cushing syndrome due to bilateral macronodular adrenocortical disease
Centre de Génétique Médicale UCL
Septo-optic dysplasia
HESX1
Septo-optic dysplasia spectrum
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Glycogen storage disease type 1a
G6PC1
Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia
Centre de Génétique Humaine - CHU Sart-Tilman
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