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 |
3439278016 | Immunodeficiency by defective expression of human leukocyte antigen class 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3439279012 | Bare lymphocyte syndrome type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3439280010 | Bare lymphocyte syndrome type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3439281014 | Immunodeficiency by defective expression of HLA (human leukocyte antigen) class 1 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3439282019 | Immunodeficiency by defective expression of human leukocyte antigen class I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5406791016 | Major histocompatibility complex class I deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5406792011 | MHC (major histocompatibility complex) class I deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5406812016 | Immunodeficiency by defective expression of human leucocyte antigen class I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5406813014 | Immunodeficiency by defective expression of human leucocyte antigen class 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5406814015 | Immunodeficiency by defective expression of HLA (human leucocyte antigen) class 1 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5407342019 | Immunodeficiency by defective expression of major histocompatibility complex class I (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5407343012 | Immunodeficiency by defective expression of major histocompatibility complex class I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403405014 | A rare autosomal recessive primary immunodeficiency characterized by severe reduction in the cell surface expression of HLA class I molecules, typically resulting in childhood-onset of chronic bacterial infections of the respiratory tract evolving to widespread bronchiectasis and respiratory insufficiency. Sterile necrotizing granulomatous skin lesions mainly involving the extremities and the mid-face may be observed in some patients. Severe viral infections do not occur as part of the condition. Atypical variants without respiratory or cutaneous manifestations, as well as asymptomatic individuals have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403406010 | A rare autosomal recessive primary immunodeficiency characterised by severe reduction in the cell surface expression of HLA class I molecules, typically resulting in childhood-onset of chronic bacterial infections of the respiratory tract evolving to widespread bronchiectasis and respiratory insufficiency. Sterile necrotising granulomatous skin lesions mainly involving the extremities and the mid-face may be observed in some patients. Severe viral infections do not occur as part of the condition. Atypical variants without respiratory or cutaneous manifestations, as well as asymptomatic individuals have been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Major histocompatibility complex class I deficiency | Is a | Autosomal recessive severe combined immunodeficiency disease (disorder) | false | Inferred relationship | Some | ||
Major histocompatibility complex class I deficiency | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
Major histocompatibility complex class I deficiency | Finding site | Body system structure | false | Inferred relationship | Some | 2 | |
Major histocompatibility complex class I deficiency | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
Major histocompatibility complex class I deficiency | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 3 | |
Major histocompatibility complex class I deficiency | Is a | Combined immunodeficiency disease | true | Inferred relationship | Some | ||
Major histocompatibility complex class I deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Immunodeficiency by defective expression of major histocompatibility complex class I due to beta-2-microglobulin mutation (disorder) | Is a | True | Major histocompatibility complex class I deficiency | Inferred relationship | Some | |
Major histocompatibility complex class I deficiency due to TAP1 mutation | Is a | True | Major histocompatibility complex class I deficiency | Inferred relationship | Some | |
Immunodeficiency by defective expression of major histocompatibility complex class I due to transporter 2, ATP binding cassette subfamily B member mutation (disorder) | Is a | True | Major histocompatibility complex class I deficiency | Inferred relationship | Some | |
Immunodeficiency by defective expression of major histocompatibility complex class I due to TAP binding protein mutation (disorder) | Is a | True | Major histocompatibility complex class I deficiency | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)