Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
42354018 | Hereditary spherocytosis due to spectrin deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
755563011 | Hereditary spherocytosis due to spectrin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Mild hereditary spherocytosis due to spectrin deficiency | Is a | True | Hereditary spherocytosis due to spectrin deficiency | Inferred relationship | Existential restriction modifier | |
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin | Is a | True | Hereditary spherocytosis due to spectrin deficiency | Inferred relationship | Existential restriction modifier | |
Severe hereditary spherocytosis due to spectrin deficiency | Is a | True | Hereditary spherocytosis due to spectrin deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets