loading...| Preferred Name |
Mucopolysaccharidosis Type I |
|
| Synonyms |
Mucopolysaccharidosis Type I Mucopolysaccharidosis I MPS I |
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| Definitions |
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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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85053 |
|
| code |
C85053 |
|
| 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). |
|
| FULL_SYN |
Mucopolysaccharidosis Type I Mucopolysaccharidosis I MPS I |
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| label |
Mucopolysaccharidosis Type I |
|
| Preferred_Name |
Mucopolysaccharidosis Type I |
|
| prefixIRI |
Thesaurus:C85053 |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0023786 |
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| subClassOf |