loading...| Preferred Name |
mucopolysaccharidosis |
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| Synonyms |
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| Definitions |
Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS]. A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine. |
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| ID |
http://purl.obolibrary.org/obo/DOID_12798 |
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| comment |
Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS]. |
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| definition |
A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine. |
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| hasAlternativeId |
DOID:14716 |
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| hasDbXref |
SNOMEDCT_US_2016_03_01:267452003 OMIM:607014 ICD10CM:E76.3 OMIM:252700 SNOMEDCT_US_2016_03_01:11380006 ORDO:79213 SNOMEDCT_US_2016_03_01:190942001 SNOMEDCT_US_2016_03_01:190936000 UMLS_CUI:C0026703 ICD9CM:277.5 MESH:D009083 NCI:C61259 |
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| hasOBONamespace |
disease_ontology |
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| id |
DOID:12798 |
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| imported from | ||
| label |
mucopolysaccharidosis |
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| prefixIRI |
DOID:12798 |
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| prefLabel |
mucopolysaccharidosis |
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| subClassOf |
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