Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Cerebral cavernous malformation (gene panel)	KRIT1, CCM2, PDCD10	Cerebral cavernous malformation (3 genes) - UCL, Vascular malformations (germline) (38 genes) - UCL	Familial cerebral cavernous malformation	Centre de Génétique Médicale UCL
Amyotrophic Lateral Sclerosis (ALS) (gene panel)		Amyotrophic Lateral Sclerosis (ALS) - UGent	Amyotrophic lateral sclerosis, Juvenile amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis type 4	Centrum Medische Genetica - UZ Gent
Amyotrophic lateral sclerosis (ALS) / Frontotemporal demention (FTD) - GGGGCC repeat expansion in C9ORF72	C9ORF72		Amyotrophic lateral sclerosis type 4, Frontotemporal dementia with motor neuron disease	Centrum Medische Genetica - UZ Gent
Atypical Hemolytic Uremic Syndrome (aHUS) (gene panel)		Atypical Hemolytic Uremic Syndrome (aHUS) and Complement disorders (16 genes) - IPG	Hemolytic uremic syndrome with DGKE deficiency, Atypical hemolytic uremic syndrome with anti-factor H antibodies, Atypical hemolytic uremic syndrome with complement gene abnormality, Atypical hemolytic-uremic syndrome with thrombomodulin anomaly, Atypical hemolytic-uremic syndrome with B factor anomaly, Atypical hemolytic-uremic syndrome with H factor anomaly, Atypical hemolytic-uremic syndrome with C3 anomaly, Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly, Atypical hemolytic-uremic syndrome with I factor anomaly	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)