Mucopolysaccharidosis Ii
Disease ID: disease_node_8762
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| Dbxref | GARD:6675, ICD10CM:E76.1, MESH:D016532, MIM:309900, NCI:C61260, SNOMEDCT_US_2023_03_01:190936000, UMLS_CUI:C0026705 |
|---|---|
| Subclassof | DOID_12798 |
| Data Source | DOID, MESH |
| Synonyms | Hunter syndrome, Hunter's syndrome, MPS II - Hunter syndrome, Mucopolysaccharidosis, MPS-II, deficiency of iduronate-2-sulphatase |
| Mesh Id | D016532 |
| Mesh Label | Mucopolysaccharidosis II |
| Mesh Subclassof | D009083, D038901 |
| Doid Label | mucopolysaccharidosis II |
| Doid Description | A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase. OMIM mapping submitted by NeuroDevNet. [LS]. |
| Disease Node Id | disease_node_8762 |
| Doid Id | DOID_12799 |
| Label | Mucopolysaccharidosis Ii |
- Outgoing r'ship
SUBCLASS_OFto/from Mucopolysaccharidoses(ID:disease_node_5259) (Disease)