| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1222.773 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.773 |
| version | 20210916 |
| status | active |
| publisher | HL7 Patient Care WG Steward |
| name | Thalassemia |
| title | Thalassemia |
| date | 2021-09-16T01:01:06-04:00 |
| experimental | false |
| description | This value set may undergo changes until the HL7 Multiple Chronic Care FHIR IG is formally published in 2024. |
| Usages | (none) |
This value set contains 90 concepts
| Code | System | Display |
| 10806241000119108 | http://snomed.info/sct | Thalassemia in mother complicating childbirth (disorder) |
| 111572002 | http://snomed.info/sct | Beta zero thalassemia non deletion type (disorder) |
| 1148897000 | http://snomed.info/sct | Hemoglobin Paksé disease (disorder) |
| 1148899002 | http://snomed.info/sct | Hemoglobin Seal Rock disease (disorder) |
| 119641000119103 | http://snomed.info/sct | Homozygous hemoglobin H constant spring thalassemia (disorder) |
| 119691000119106 | http://snomed.info/sct | Hemoglobin C/beta thalassemia disease (disorder) |
| 119701000119106 | http://snomed.info/sct | Hemoglobin D/beta thalassemia disease (disorder) |
| 127041004 | http://snomed.info/sct | Sickle cell-beta-thalassemia (disorder) |
| 127042006 | http://snomed.info/sct | Sickle cell beta plus thalassemia (disorder) |
| 127043001 | http://snomed.info/sct | Sickle cell-beta^0^-thalassemia (disorder) |
| 127044007 | http://snomed.info/sct | Sickle cell-delta beta^0^-thalassemia (disorder) |
| 127045008 | http://snomed.info/sct | Sickle cell anemia with coexistent alpha-thalassemia (disorder) |
| 127046009 | http://snomed.info/sct | Sickle cell trait with coexistent alpha-thalassemia (disorder) |
| 15326009 | http://snomed.info/sct | beta^+^ Thalassemia, normal Hb A>2<, type 2 (disorder) |
| 16360009 | http://snomed.info/sct | Delta beta thalassemia (disorder) |
| 16427007 | http://snomed.info/sct | Delta thalassemia (disorder) |
| 16964007 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin thalassemia (disorder) |
| 191187006 | http://snomed.info/sct | Alpha trait thalassemia (disorder) |
| 191189009 | http://snomed.info/sct | Beta thalassemia intermedia (disorder) |
| 19442009 | http://snomed.info/sct | Heterozygous thalassemia (disorder) |
| 23371004 | http://snomed.info/sct | Epsilon gamma delta beta thalassemia (disorder) |
| 234383000 | http://snomed.info/sct | Homozygous alpha thalassemia (disorder) |
| 234385007 | http://snomed.info/sct | Alpha thalassemia-2 trait (disorder) |
| 234386008 | http://snomed.info/sct | Hemoglobin Constant Spring trait (disorder) |
| 234387004 | http://snomed.info/sct | Hemoglobin Lepore trait (disorder) |
| 234388009 | http://snomed.info/sct | Delta-beta-Lepore thalassemia (disorder) |
| 234389001 | http://snomed.info/sct | Alpha-beta thalassemia (disorder) |
| 234390005 | http://snomed.info/sct | Gamma thalassemia (disorder) |
| 234392002 | http://snomed.info/sct | Hemoglobin E/beta thalassemia disease (disorder) |
| 26682008 | http://snomed.info/sct | Homozygous beta thalassemia (disorder) |
| 269175006 | http://snomed.info/sct | Beta thalassemia trait (disorder) |
| 27080008 | http://snomed.info/sct | Beta zero thalassemia deletion type (disorder) |
| 307343001 | http://snomed.info/sct | Acquired hemoglobin H disease (disorder) |
| 32855007 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder) |
| 36467003 | http://snomed.info/sct | Alpha plus thalassemia (disorder) |
| 36472007 | http://snomed.info/sct | Sickle cell-thalassemia disease (disorder) |
| 39586009 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) |
| 40108008 | http://snomed.info/sct | Thalassemia (disorder) |
| 416826005 | http://snomed.info/sct | Sickle cell-thalassemia disease with crisis (disorder) |
| 417048006 | http://snomed.info/sct | Sickle cell-thalassemia disease without crisis (disorder) |
| 447117006 | http://snomed.info/sct | Hemoglobin H constant spring thalassemia (disorder) |
| 47047009 | http://snomed.info/sct | Thalassemia with other hemoglobinopathy (disorder) |
| 47084006 | http://snomed.info/sct | Beta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder) |
| 48553001 | http://snomed.info/sct | Hemoglobin H disease (disorder) |
| 5300004 | http://snomed.info/sct | Hemoglobin Bart's hydrops syndrome (disorder) |
| 54006005 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) |
| 56205004 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin, nondeletion type (disorder) |
| 5967006 | http://snomed.info/sct | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder) |
| 61395005 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) |
| 61777009 | http://snomed.info/sct | Thalassemia-hemoglobin C disease (disorder) |
| 62074008 | http://snomed.info/sct | Delta zero thalassemia (disorder) |
| 65959000 | http://snomed.info/sct | Beta thalassemia (disorder) |
| 66055002 | http://snomed.info/sct | Alpha zero thalassemia (disorder) |
| 68913001 | http://snomed.info/sct | Alpha thalassemia (disorder) |
| 69216008 | http://snomed.info/sct | Hb Lepore thalassemia (disorder) |
| 715342005 | http://snomed.info/sct | Alpha thalassemia X-linked intellectual disability syndrome (disorder) |
| 716682000 | http://snomed.info/sct | Dominant beta-thalassemia (disorder) |
| 718196002 | http://snomed.info/sct | Beta thalassemia X-linked thrombocytopenia syndrome (disorder) |
| 72331000119105 | http://snomed.info/sct | Thalassemia in mother complicating pregnancy (disorder) |
| 73190000 | http://snomed.info/sct | Epsilon gamma delta beta^0^ thalassemia (disorder) |
| 734349003 | http://snomed.info/sct | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) |
| 75451007 | http://snomed.info/sct | Thalassemia major (disorder) |
| 76336008 | http://snomed.info/sct | Delta beta zero thalassemia (disorder) |
| 788944005 | http://snomed.info/sct | Gamma delta beta thalassemia (disorder) |
| 79592006 | http://snomed.info/sct | Beta plus thalassemia (disorder) |
| 84188003 | http://snomed.info/sct | Thalassemia syndrome (disorder) |
| 85422000 | http://snomed.info/sct | Alpha plus thalassemia non deletion type (disorder) |
| 85557000 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin deletion type (disorder) |
| 86242003 | http://snomed.info/sct | Alpha plus thalassemia deletion type (disorder) |
| 86715000 | http://snomed.info/sct | Beta zero thalassemia (disorder) |
| 89459006 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster (disorder) |
| 89810003 | http://snomed.info/sct | ^A^gamma delta beta^0^ thalassemia (disorder) |
| 934007 | http://snomed.info/sct | Thalassemia intermedia (disorder) |
| D56 | http://hl7.org/fhir/sid/icd-10-cm | Thalassemia |
| D56.0 | http://hl7.org/fhir/sid/icd-10-cm | Alpha thalassemia |
| D56.1 | http://hl7.org/fhir/sid/icd-10-cm | Beta thalassemia |
| D56.2 | http://hl7.org/fhir/sid/icd-10-cm | Delta-beta thalassemia |
| D56.3 | http://hl7.org/fhir/sid/icd-10-cm | Thalassemia minor |
| D56.4 | http://hl7.org/fhir/sid/icd-10-cm | Hereditary persistence of fetal hemoglobin [HPFH] |
| D56.5 | http://hl7.org/fhir/sid/icd-10-cm | Hemoglobin E-beta thalassemia |
| D56.8 | http://hl7.org/fhir/sid/icd-10-cm | Other thalassemias |
| D56.9 | http://hl7.org/fhir/sid/icd-10-cm | Thalassemia, unspecified |
| D57.2 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease |
| D57.20 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease without crisis |
| D57.21 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease with crisis |
| D57.211 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease with acute chest syndrome |
| D57.212 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease with splenic sequestration |
| D57.213 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease with cerebral vascular involvement |
| D57.218 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease with crisis with other specified complication |
| D57.219 | http://hl7.org/fhir/sid/icd-10-cm | Sickle-cell/Hb-C disease with crisis, unspecified |
Produced 08 Sep 2023