Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3505250016 | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3505251017 | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3505252012 | Alpha-thalassaemia intellectual disability syndrome linked to chromosome 16 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3505253019 | ATR-16 syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3505254013 | Alpha thalassemia intellectual disability syndrome, deletion type | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3505255014 | Alpha thalassaemia intellectual disability syndrome, deletion type | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403883013 | A rare developmental defect during embryogenesis, a contiguous gene deletion syndrome, is a form of alpha-thalassemia characterized by microcytosis, hypochromia, normal hemoglobin (Hb) level or mild anemia, associated with developmental abnormalities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403884019 | A rare developmental defect during embryogenesis, a contiguous gene deletion syndrome, is a form of alpha-thalassaemia characterised by microcytosis, hypochromia, normal haemoglobin (Hb) level or mild anaemia, associated with developmental abnormalities. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Alpha thalassemia (disorder) | true | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Mental retardation | false | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Deletion of part of short arm of chromosome 16 (disorder) | true | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Finding site | Chromosome pair 16 | false | Inferred relationship | Some | 5 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 6 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 7 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 8 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 8 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 9 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Interprets | Red blood cell count | true | Inferred relationship | Some | 9 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Associated morphology | Deletion of short arm | false | Inferred relationship | Some | 6 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Finding site | Chromosome pair 16 | false | Inferred relationship | Some | 6 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Some | 7 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Associated morphology | Partial monosomy (morphologic abnormality) | false | Inferred relationship | Some | 5 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Finding site | Short arm of chromosome | true | Inferred relationship | Some | 1 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Associated morphology | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Congenital malformation | true | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Finding site | Chromosome pair 16 | true | Inferred relationship | Some | 2 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Associated morphology | Partial monosomy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Is a | Congenital anemia | true | Inferred relationship | Some | ||
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 6 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 6 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 3 | |
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)