Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
44770015 | Mucopolysaccharidosis, MPS-I-H/S | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
44771016 | Hurler-Scheie syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
44772011 | L-iduronidase deficiency, Hurler-Scheie type | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
483333016 | Hurler-Scheie disease MPS type 1H/S | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
2971450019 | Mucopolysaccharidosis type I-H/S (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2971919011 | Mucopolysaccharidosis type I-H/S | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Mucopolysaccharidosis, MPS-I-H/S | Is a | Mucopolysaccharidosis, MPS-I | true | Inferred relationship | Some | ||
Mucopolysaccharidosis, MPS-I-H/S | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Mucopolysaccharidosis, MPS-I-H/S | Finding site | Body system structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets