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 |
| 42354018 | Hereditary spherocytosis due to spectrin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 42355017 | Hereditary spherocytosis due to spectrin deficiency, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 755563011 | Hereditary spherocytosis due to spectrin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Mild hereditary spherocytosis due to spectrin deficiency | est un(e) (attribut) | True | Hereditary spherocytosis due to spectrin deficiency | Inferred relationship | Some | |
| Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) | est un(e) (attribut) | True | Hereditary spherocytosis due to spectrin deficiency | Inferred relationship | Some | |
| Severe hereditary spherocytosis due to spectrin deficiency | est un(e) (attribut) | True | Hereditary spherocytosis due to spectrin deficiency | Inferred relationship | Some |
Reference Sets