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Disease Ontology Browser
mucopolysaccharidosis I (DOID:12802)
Synonyms: Hurler syndrome; Hurler-Scheie syndrome; iduronidase deficiency disease; Lipochondrodystrophy; MPS I - Hurler syndrome; Mucopolysaccharidosis, MPS-I (disorder); Mucopolysaccharidosis, type 1
Alt IDs: OMIM:607014, OMIM:607015, OMIM:607016, ICD10CM:E76.0, MESH:D008059, NCI:C85053, UMLS_CUI:C0023786
Definition: A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme alpha-L-iduronidase.

Disease References using Mouse Models (23)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/20/2017
MGI 6.10
The Jackson Laboratory