loading...| Preferred Name |
Mucopolysaccharidosis Type I |
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| Synonyms |
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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Mucopolysaccharidosis_Type_I |
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| 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). |
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| FULL_SYN |
Mucopolysaccharidosis I |
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| isDefinedBy |
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). |
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| label |
Mucopolysaccharidosis Type I |
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| prefixIRI |
Thesaurus:Mucopolysaccharidosis_Type_I |
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| prefLabel |
Mucopolysaccharidosis Type I |
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| Synonym |
Mucopolysaccharidosis I |
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| subClassOf |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Mucopolysaccharidosis |