Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
398839012 | Lactose intolerance | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
398840014 | LM - Lactose malabsorption | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
398841013 | Cow's milk enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
398842018 | Lactose malabsorption | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
660040013 | Lactose intolerance (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2031031000005115 | Laktoseintolerans | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Laktoseintolerans | Is a | Disorder of carbohydrate absorption | false | Inferred relationship | Some | ||
Laktoseintolerans | Is a | Disorder of intestine | false | Inferred relationship | Some | ||
Laktoseintolerans | Finding site | Intestinal structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Primary lactose intolerance | Is a | False | Laktoseintolerans | Inferred relationship | Some | |
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. | Is a | False | Laktoseintolerans | Inferred relationship | Some | |
Lactase deficiency in diseases other than of the small intestine | Is a | False | Laktoseintolerans | Inferred relationship | Some | |
Nonpersistence of intestinal lactase | Is a | False | Laktoseintolerans | Inferred relationship | Some | |
Congenital lactase deficiency | Is a | False | Laktoseintolerans | Inferred relationship | Some | |
Intolerance to lactose in children without lactase deficiency (finding) | Is a | False | Laktoseintolerans | Inferred relationship | Some | |
Acquired lactase deficiency | Is a | False | Laktoseintolerans | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)