Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3444183015 | Congenital enterocyte heparan sulfate deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444184014 | Congenital enterocyte heparan sulfate deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3444185010 | Congenital enterocyte heparan sulphate deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403494017 | A rare, severe, genetic, intestinal disease characterized by congenital absence of heparan sulfate from small intestine epithelium manifesting with secretory diarrhea and massive enteric protein loss. Patients present intolerance to enteral feeds during the first few weeks to months of life. Apart from absence of heparan sulfate from the basolateral surface of small intestine enterocytes, small bowel biopsy is otherwise normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403495016 | A rare, severe, genetic, intestinal disease characterised by congenital absence of heparan sulfate from small intestine epithelium manifesting with secretory diarrhoea and massive enteric protein loss. Patients present intolerance to enteral feeds during the first few weeks to months of life. Apart from absence of heparan sulfate from the basolateral surface of small intestine enterocytes, small bowel biopsy is otherwise normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital enterocyte heparan sulfate deficiency (disorder) | Is a | Congenital anomaly of intestinal tract | true | Inferred relationship | Some | ||
Congenital enterocyte heparan sulfate deficiency (disorder) | Is a | Disorder of gastrointestinal tract mucous membrane (disorder) | true | Inferred relationship | Some | ||
Congenital enterocyte heparan sulfate deficiency (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
Congenital enterocyte heparan sulfate deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital enterocyte heparan sulfate deficiency (disorder) | Finding site | Intestinal mucous membrane structure | true | Inferred relationship | Some | 1 | |
Congenital enterocyte heparan sulfate deficiency (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital enterocyte heparan sulfate deficiency (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Congenital enterocyte heparan sulfate deficiency (disorder) | Is a | Disorder of soft tissue of trunk | false | Inferred relationship | Some | ||
Congenital enterocyte heparan sulfate deficiency (disorder) | Is a | Disorder of soft tissue of abdominal cavity | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)