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description: Conditions markedly more frequent in people of Ashkenazi Jewish ancestry, where founder mutations are unusually well characterised. A prevalence signal, not an exclusive one.
locale: en
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Tay-Sachs Disease
Gaucher Disease Type 1
Familial Dysautonomia
Canavan Disease
Niemann-Pick Disease Type A
Bloom Syndrome
Factor XI Deficiency
BRCA1 Founder Mutation
BRCA2 Founder Mutation
Mucolipidosis Type IV
Crohn Disease
Torsion Dystonia
