loading...| Preferred Name | mucopolysaccharidosis | |
| Synonyms |
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| Definitions |
A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine. Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_12798 |
|
| comment |
Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS]. |
|
| database_cross_reference |
SNOMEDCT_US_2023_03_01:267452003 ICD9CM:277.5 ICD10CM:E76.3 MESH:D009083 UMLS_CUI:C0026703 MIM:PS607014 GARD:7065 NCI:C61259 ORDO:79213 |
|
| definition |
A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine. Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS]. |
|
| has_alternative_id |
DOID:14716 |
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| has_obo_namespace |
disease_ontology |
|
| id |
DOID:12798 |
|
| in_subset | ||
| label |
mucopolysaccharidosis |
|
| notation |
DOID:12798 |
|
| note |
A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine. Xref MGI. OMIM mapping submitted by NeuroDevNet. [LS]. |
|
| preferred label |
mucopolysaccharidosis |
|
| prefLabel |
mucopolysaccharidosis |
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| subClassOf |