Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 43143014 | Hereditary gastrogenic lactose intolerance | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 43144015 | Severe familial lactose intolerance | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 756097018 | Hereditary gastrogenic lactose intolerance (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3754810012 | A very rare disorder which is probably hereditary. It is not caused by a disorder of disaccharidease activity or by impairment of monosaccharide transport but rather by abnormal permeability of lactose through the gastric mucosa. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set