Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4696480011 | 2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696481010 | OAS1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4696482015 | Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4696483013 | OAS1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4696484019 | Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696485018 | 2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696486017 | Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
4696487014 | A rare genetic respiratory disease characterized by infantile onset of pulmonary alveolar proteinosis with hypogammaglobulinemia. Patients have normal respiratory function at birth, but subsequently develop recurrent, mainly viral, infections and progressive respiratory failure, often leading to death in infancy or early childhood. Additional reported features include leukocytosis and splenomegaly. | en | Definition | Active | Case sensitive | SNOMED CT core |
4696488016 | A rare genetic respiratory disease characterised by infantile onset of pulmonary alveolar proteinosis with hypogammaglobulinaemia. Patients have normal respiratory function at birth, but subsequently develop recurrent, mainly viral, infections and progressive respiratory failure, often leading to death in infancy or early childhood. Additional reported features include leucocytosis and splenomegaly. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Pulmonary alveolar proteinosis | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Hypogammaglobulinaemia | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Primary immune deficiency disorder | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Genetic disease | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 4 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Interprets | Globulin measurement | true | Inferred relationship | Some | 2 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Finding site | Pulmonary alveolar structure | true | Inferred relationship | Some | 1 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Associated morphology | Protein deposition | true | Inferred relationship | Some | 1 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Chronic inflammatory disorder | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Chronic disease of immune function | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Is a | Chronic lung disease | true | Inferred relationship | Some | ||
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Clinical course | Chronic | true | Inferred relationship | Some | 5 | |
Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia | Associated morphology | Chronic inflammatory morphology | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Respiratory finding reference set
Problem/Diagnosis reference set