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Facioscapulohumeral muscular dystrophy 1A (D4Z4 repeat)
FRG1
Facioscapulohumeral dystrophy
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Facioscapulohumeral Muscular Dystrophy 2 (hypomethylation D4Z4 repeats)
FRG1
Facioscapulohumeral dystrophy
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Facioscapulohumeral muscular dystrophy 1A (D4Z4 repeat)
FRG1
Facioscapulohumeral dystrophy
Centrum Menselijke Erfelijkheid - KUL
Fanconi anemia (gene panel)
Fanconi anemia - UGent
Fanconi anemia
Centrum Medische Genetica - UZ Gent
Fanconi anemia (FANCC) (hot spot mutation - c.456+4A>T)
FANCC
Fanconi anemia
Centrum Medische Genetica - UZ Antwerpen
Immunodeficiency 30 / Susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
IL12RB1
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Centrum Menselijke Erfelijkheid - KUL
Leber Congenital Amaurosis - Retinal dystrophy, early onset (gene panel)
Leber Congenital Amaurosis - UGent
Leber congenital amaurosis
,
Cone rod dystrophy
,
Retinitis pigmentosa
,
Senior-Loken syndrome
,
Severe early-childhood-onset retinal dystrophy
Centrum Medische Genetica - UZ Gent
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