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 |
3434639011 | Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434640013 | Hepatic veno-occlusive disease with immunodeficiency syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3434641012 | VODI (veno-occlusive disease, immunodeficiency) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3434642017 | VODI syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
760511000241112 | syndrome de maladie veino-occlusive hépatique-immunodéficience (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
999041000172110 | syndrome de maladie veino-occlusive hépatique-immunodéficience | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
3434643010 | Syndrome that is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding PML nuclear body protein Sp110 on chromosome 2q37 were found to be responsible for this association. Transmission is autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3434644016 | Syndrome that is characterised by the association of severe hypogammaglobulinaemia, combined T and B cell immunodeficiency, absent lymph node germinal centres, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding PML nuclear body protein Sp110 on chromosome 2q37 were found to be responsible for this association. Transmission is autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 2 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est un(e) (attribut) | Severe combined immunodeficiency with low T- and B-cell numbers | true | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | localisation d'une constatation (attribut) | structure du système immunitaire | true | Inferred relationship | Some | 2 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | localisation d'une constatation (attribut) | Structure of hepatic vein | true | Inferred relationship | Some | 1 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 2 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | morphologie associée (attribut) | obstruction | true | Inferred relationship | Some | 1 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est un(e) (attribut) | Veno-occlusive disease of the liver | true | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est un(e) (attribut) | Autosomal recessive severe combined immunodeficiency disease (disorder) | true | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est un(e) (attribut) | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est un(e) (attribut) | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est un(e) (attribut) | Congenital vascular disorder (disorder) | false | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | est défini par la manifestation de (attribut) | Immune system finding | false | Inferred relationship | Some | ||
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | morphologie associée (attribut) | obstruction | false | Inferred relationship | Some | 3 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 3 | |
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) | localisation d'une constatation (attribut) | Structure of hepatic vein | false | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets