Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3724272019 | Congenital chronic diarrhea with protein-losing enteropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3724273012 | Congenital chronic diarrhea with exudative enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3724274018 | Congenital chronic diarrhoea with protein-losing enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3724275017 | Congenital chronic diarrhea with protein-losing enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3724276016 | Congenital chronic diarrhoea with exudative enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6202831000146113 | congenitale chronische diarree met 'protein-losing enteropathy' | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6202841000146117 | congenitale chronische diarree met 'protein-losing' enteropathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6202851000146119 | congenitale chronische diarree met 'protein-losing enteropathy' (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6202861000146116 | aangeboren chronische diarree met exsudatieve enteropathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3724841010 | A rare genetic intestinal disease characterised by early-onset chronic non-infectious, non-bloody, watery diarrhoea associated with protein-losing enteropathy, which results in hypoalbuminaemia, hypogammaglobulinaemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhoea, failure to thrive, recurrent infections and oedema. There is evidence the disease is caused by homozygous mutation in the DGAT1 gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3724842015 | A rare genetic intestinal disease characterized by early-onset chronic non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy, which results in hypoalbuminemia, hypogammaglobulinemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhea, failure to thrive, recurrent infections and edema. There is evidence the disease is caused by homozygous mutation in the DGAT1 gene. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Interprets | Bowel action | true | Inferred relationship | Some | 2 | |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Clinical course | Chronic | true | Inferred relationship | Some | 3 | |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Has interpretation | Altered | true | Inferred relationship | Some | 2 | |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Chronic diarrhea of infants AND/OR young children | true | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Congenital disease (disorder) | false | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Protein-losing enteropathy | true | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Finding site | Structure of small intestine (body structure) | true | Inferred relationship | Some | 1 | |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Interprets | Digestive system function | false | Inferred relationship | Some | 4 | |
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Diarrheal disorder | true | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Disorder of digestive system specific to fetus OR newborn | false | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Congenital disorder of intestine (disorder) | true | Inferred relationship | Some | ||
| Congenital chronic diarrhea with protein-losing enteropathy (disorder) | Is a | Congenital diarrhea (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR