Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
206335017 | Structural hemoglobinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
326013 | Hereditary hemoglobinopathy due to globin chain mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
474018017 | Hereditary haemoglobinopathy due to globin chain mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
474019013 | Structural haemoglobinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
731076011 | Hereditary hemoglobinopathy due to globin chain mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Unstable hemoglobin disease | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
hémoglobinose E (trouble) | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Haemoglobin E trait | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
hémoglobinose C (trouble) | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Hemoglobin D disease | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Hemoglobin D trait | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Hemoglobin M disease | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Hemoglobin C trait | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Hereditary hemoglobin S (disorder) | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Congenital methemoglobinemia with abnormal methemoglobins | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
Hemoglobin O-Arab trait (disorder) | est un(e) (attribut) | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some |
This concept is not in any reference sets