| Name | Value | Comments |
|---|
 compose.inactive | | |
| compose.lockedDate | | |
| copyright | This value set includes content from SNOMED CT, which is copyright © 2002+ International Health Terminology Standards Development Organisation (IHTSDO), and distributed by agreement between IHTSDO and HL7. Implementer use of SNOMED CT is not covered by this agreement | |
| date | 2021-12-08T02:47:19+00:00 | 2022-07-25T13:21:55+00:00 | |
| description | A set of codes that describe underlying hemoglobinopathy conditions for COVID19 | |
| experimental | | |
| immutable | | |
| jurisdiction | | |
 jurisdiction[0] | urn:iso:std:iso:3166#US | |
| name | COVID19UnderlyingHemoglobinopathyConditionVS | |
| publisher | HL7 International - Clinical Information Modeling Initiative | |
| purpose | | |
| status | active | |
| title | COVID-19 hemoglobinopathy underlying condition reference set | |
| url | http://hl7.org/fhir/us/covid19library/ValueSet/covid91-underlying-hemoglobinopathy-condition-value-set | |
| version | 0.14.0 | 1.0.0 | |
| Item | Property | Value | Comments |
|---|
| include | http://snomed.info/sct | | |
 Concept | 68913001 | Alpha thalassemia (disorder) | Alpha thalassemia (disorder) | |
| Concept | 36351005 | Antithrombin III deficiency (disorder) | |
| Concept | 306058006 | Aplastic anemia (disorder) | Aplastic anemia (disorder) | |
| Concept | 707147002 | Asplenia (disorder) | Asplenia (disorder) | |
| Concept | 65959000 | Beta thalassemia (disorder) | Beta thalassemia (disorder) | |
| Concept | 64779008 | Blood coagulation disorder (disorder) | Blood coagulation disorder (disorder) | |
| Concept | 715559004 | Combined deficiency of factor V and factor VIII (disorder) | |
| Concept | 767712006 | Factor IX deficiency (disorder) | |
| Concept | 4320005 | Factor V deficiency (disorder) | |
| Concept | 307091009 | Factor V Leiden mutation (disorder) | |
| Concept | 37193007 | Factor VII deficiency (disorder) | |
| Concept | 76642003 | Factor X deficiency (disorder) | |
| Concept | 767713001 | Factor XI deficiency (disorder) | |
| Concept | 359727008 | Fibrinogen deficiency (disorder) | |
| Concept | 90935002 | Hemophilia (disorder) | |
| Concept | 41788008 | Hereditary factor IX deficiency disease (disorder) | |
| Concept | 28293008 | Hereditary factor VIII deficiency disease (disorder) | |
| Concept | 49762007 | Hereditary factor XI deficiency disease (disorder) | |
| Concept | 84828003 | Leukopenia (disorder) | Leukopenia (disorder) | |
| Concept | 109995007 | Myelodysplastic syndrome (disorder) | |
| Concept | 165517008 | Neutropenia (finding) | Neutropenia (finding) | |
| Concept | 127034005 | Pancytopenia (disorder) | Pancytopenia (disorder) | |
| Concept | 109992005 | Polycythemia vera (disorder) | Polycythemia vera (disorder) | |
| Concept | 76407009 | Protein C deficiency disease (disorder) | |
| Concept | 1563006 | Protein S deficiency disease (disorder) | |
| Concept | 440989002 | Prothrombin G20210A mutation (disorder) | |
| Concept | 127041004 | Sickle cell-beta-thalassemia (disorder) | Sickle cell-beta-thalassemia (disorder) | |
| Concept | 127040003 | Sickle cell-hemoglobin SS disease (disorder) | Sickle cell-hemoglobin SS disease (disorder) | |
| Concept | 417357006 | Sickling disorder due to hemoglobin S (disorder) | |
| Concept | 302215000 | Thrombocytopenic disorder (disorder) | Thrombocytopenic disorder (disorder) | |
| Concept | 128105004 | von Willebrand disorder (disorder) | |
| Code | Display | Comments |
|---|
| 68913001 | Alpha thalassemia (disorder) | Alpha thalassemia (disorder) | - display changed from left to right
|
| 36351005 | Antithrombin III deficiency (disorder) | |
| 306058006 | Aplastic anemia (disorder) | Aplastic anemia (disorder) | - display changed from left to right
|
| 707147002 | Asplenia (disorder) | Asplenia (disorder) | - display changed from left to right
|
| 65959000 | Beta thalassemia (disorder) | Beta thalassemia (disorder) | - display changed from left to right
|
| 64779008 | Blood coagulation disorder (disorder) | Blood coagulation disorder (disorder) | - display changed from left to right
|
| 715559004 | Combined deficiency of factor V and factor VIII (disorder) | |
| 767712006 | Factor IX deficiency (disorder) | |
| 4320005 | Factor V deficiency (disorder) | |
| 307091009 | Factor V Leiden mutation (disorder) | |
| 37193007 | Factor VII deficiency (disorder) | |
| 76642003 | Factor X deficiency (disorder) | |
| 767713001 | Factor XI deficiency (disorder) | |
| 359727008 | Fibrinogen deficiency (disorder) | |
| 90935002 | Hemophilia (disorder) | |
| 41788008 | Hereditary factor IX deficiency disease (disorder) | |
| 28293008 | Hereditary factor VIII deficiency disease (disorder) | |
| 49762007 | Hereditary factor XI deficiency disease (disorder) | |
| 84828003 | Leukopenia (disorder) | Leukopenia (disorder) | - display changed from left to right
|
| 109995007 | Myelodysplastic syndrome (disorder) | |
| 165517008 | Neutropenia (finding) | Neutropenia (finding) | - display changed from left to right
|
| 127034005 | Pancytopenia (disorder) | Pancytopenia (disorder) | - display changed from left to right
|
| 109992005 | Polycythemia vera (disorder) | Polycythemia vera (disorder) | - display changed from left to right
|
| 76407009 | Protein C deficiency disease (disorder) | |
| 1563006 | Protein S deficiency disease (disorder) | |
| 440989002 | Prothrombin G20210A mutation (disorder) | |
| 127041004 | Sickle cell-beta-thalassemia (disorder) | Sickle cell-beta-thalassemia (disorder) | - display changed from left to right
|
| 127040003 | Sickle cell-hemoglobin SS disease (disorder) | Sickle cell-hemoglobin SS disease (disorder) | - display changed from left to right
|
| 417357006 | Sickling disorder due to hemoglobin S (disorder) | |
| 302215000 | Thrombocytopenic disorder (disorder) | Thrombocytopenic disorder (disorder) | - display changed from left to right
|
| 128105004 | von Willebrand disorder (disorder) | |