Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3303733010 | Progressive encephalopathy with severe infantile anorexia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303734016 | Progressive encephalopathy with severe infantile anorexia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303735015 | RAVINE syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3303736019 | RAVINE syndrome is an extremely rare genetic neurological disorder reported in a small number of patients in a specific community on Reunion Island (France) with manifestation of infantile anorexia, irrepressible and repeated vomiting, acute brainstem dysfunction, severe failure to thrive, and progressive encephalopathy with MRI showing vanishing of posterior fossa along with supra-tentorial periventricular white-matter hyperintensities and basal ganglion anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Progressive encephalopathy with severe infantile anorexia (disorder) | est un(e) (attribut) | Leukodystrophy | true | Inferred relationship | Some | ||
| Progressive encephalopathy with severe infantile anorexia (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Progressive encephalopathy with severe infantile anorexia (disorder) | morphologie associée (attribut) | Myelin sheath alteration | true | Inferred relationship | Some | 1 | |
| Progressive encephalopathy with severe infantile anorexia (disorder) | localisation d'une constatation (attribut) | système nerveux | false | Inferred relationship | Some | 1 | |
| Progressive encephalopathy with severe infantile anorexia (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Progressive encephalopathy with severe infantile anorexia (disorder) | localisation d'une constatation (attribut) | White matter structure of brain and spinal cord (body structure) | true | Inferred relationship | Some | 2 | |
| Progressive encephalopathy with severe infantile anorexia (disorder) | localisation d'une constatation (attribut) | Myelinated nerve fiber structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR