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Disease association ontology term - MONDO:0001586 - mucopolysaccharidosis type 1

Term summary

ID
MONDO:0001586
Name
mucopolysaccharidosis type 1
Ontology or CV name
Disease association
Definition
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).

Parents

Annotation