Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1231551018 | HS - Hereditary spherocytosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
497486018 | Congenital spherocytic haemolytic anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
794457015 | Hereditary spherocytosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
93126010 | Hereditary spherocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
93128011 | Familial spherocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
93129015 | Minkowsky-Chauffard syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
93130013 | Congenital spherocytosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
93131012 | Familial acholuric jaundice | en | Synonym | Active | Case insensitive | SNOMED CT core |
93132017 | Congenital spherocytic hemolytic anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set