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 |
3424876017 | RAS-associated autoimmune leukoproliferative disease (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424877014 | RAS-associated autoimmune leukoproliferative disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424878016 | RAS-associated autoimmune leucoproliferative disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424879012 | Autoimmune lymphoproliferative syndrome type 4 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3424880010 | Autoimmune lymphoproliferative syndrome type IV | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3424881014 | RALD - RAS-associated autoimmune leukoproliferative disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3424882019 | RALD - RAS-associated autoimmune leucoproliferative disease | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403095014 | RAS-associated autoimmune leukoproliferative disease (RALD) is a rare genetic disorder characterized by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinemia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403096010 | RAS-associated autoimmune leucoproliferative disease (RALD) is a rare genetic disorder characterised by monocytosis, autoimmune cytopenias, lymphoproliferation, hepatosplenomegaly, and hypergammaglobulinaemia. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
RAS-associated autoimmune leukoproliferative disease (disorder) | Due to | Chromosomal disorder (disorder) | true | Inferred relationship | Some | 2 | |
RAS-associated autoimmune leukoproliferative disease (disorder) | Is a | Autoimmune disease | true | Inferred relationship | Some | ||
RAS-associated autoimmune leukoproliferative disease (disorder) | Is a | Immunodeficiency associated with chromosomal abnormality | true | Inferred relationship | Some | ||
RAS-associated autoimmune leukoproliferative disease (disorder) | Is a | Lymphoproliferative disorder | true | Inferred relationship | Some | ||
RAS-associated autoimmune leukoproliferative disease (disorder) | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Some | ||
RAS-associated autoimmune leukoproliferative disease (disorder) | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
RAS-associated autoimmune leukoproliferative disease (disorder) | Associated morphology | Lymphoproliferative disorder (morphologic abnormality) | true | Inferred relationship | Some | 4 | |
RAS-associated autoimmune leukoproliferative disease (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)