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- Be3ea643dcedebb661f476ba9f383f039 hasDbXref "NCIT:P378" @default.
- Be3ea643dcedebb661f476ba9f383f039 type Axiom @default.
- Be3ea643dcedebb661f476ba9f383f039 annotatedProperty IAO_0000115 @default.
- Be3ea643dcedebb661f476ba9f383f039 annotatedSource MONDO_0001586 @default.
- Be3ea643dcedebb661f476ba9f383f039 annotatedTarget "The most common type of mucopolysaccharidosis. It is inherited in an autosomal recessive pattern. It comprises a group of lysosomal storage diseases which includes the most severe form (Hurler syndrome) and the mildest form (Scheie syndrome)." @default.