Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3758297010 | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3758298017 | Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3758299013 | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | Finding site | Erythrocyte | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | Is a | Hereditary persistence of fetal hemoglobin | true | Inferred relationship | Existential restriction modifier | ||
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome | Is a | Sickling disorder due to hemoglobin S | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets