Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5048470018 | Interstitial lung disease due to ABCA3 (ATP-binding cassette subfamily A member 3) deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5048471019 | Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5048472014 | Interstitial lung disease due to ABCA3 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5048517014 | Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5048473016 | A rare genetic respiratory disease with characteristics of a variable clinical outcome ranging from a fatal respiratory distress syndrome in the neonatal period to chronic interstitial lung disease developing in infancy or childhood with chronic cough, rapid breathing, shortness of breath and recurrent pulmonary infections. Clinical manifestations of respiratory failure include grunting, intercostal retractions, nasal flaring, cyanosis, and progressive dyspnoea. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5048474010 | A rare genetic respiratory disease with characteristics of a variable clinical outcome ranging from a fatal respiratory distress syndrome in the neonatal period to chronic interstitial lung disease developing in infancy or childhood with chronic cough, rapid breathing, shortness of breath and recurrent pulmonary infections. Clinical manifestations of respiratory failure include grunting, intercostal retractions, nasal flaring, cyanosis, and progressive dyspnea. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder) | est un(e) (attribut) | Connective tissue hereditary disorder | true | Inferred relationship | Some | ||
| Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder) | est un(e) (attribut) | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder) | localisation d'une constatation (attribut) | structure du tissu interstitiel du poumon | true | Inferred relationship | Some | 1 | |
| Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder) | est un(e) (attribut) | pneumopathie interstitielle | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
Description inactivation indicator reference set
FHIR