FHIR IG Statistics: ValueSet/2.16.840.1.113762.1.4.1029.286
| Package | us.nlm.vsac |
| Resource Type | ValueSet |
| Id | 2.16.840.1.113762.1.4.1029.286 |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1029.286/expansion |
| URL | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1029.286 |
| Version | 20230217 |
| Status | active |
| Date | 2023-02-17T01:03:27-05:00 |
| Name | BleedingDisorder |
| Title | Bleeding Disorder |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: The purpose of this value set is to identify diagnoses of bleeding disorders.),(Data Element Scope: This value set may use a model element related to diagnosis.),(Inclusion Criteria: Includes concepts that identify a diagnosis of a bleeding disorder.),(Exclusion Criteria: No exclusions.) |
Resources that use this resource
Resources that this resource uses
| CodeSystem |
| icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
Narrative
No narrative content found in resource
Source
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"display": "Hereditary factor VIII deficiency"
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{
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"display": "Hereditary factor IX deficiency"
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{
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"display": "Acquired von Willebrand disease"
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{
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"display": "Hemorrhagic disorder due to extrinsic circulating anticoagulants"
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{
"code": "D68.4",
"display": "Acquired coagulation factor deficiency"
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{
"code": "D68.51",
"display": "Activated protein C resistance"
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"display": "Prothrombin gene mutation"
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{
"code": "D68.59",
"display": "Other primary thrombophilia"
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{
"code": "D68.61",
"display": "Antiphospholipid syndrome"
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{
"code": "D68.62",
"display": "Lupus anticoagulant syndrome"
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{
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"display": "Other thrombophilia"
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{
"code": "D69.0",
"display": "Allergic purpura"
},
{
"code": "D69.1",
"display": "Qualitative platelet defects"
},
{
"code": "D69.2",
"display": "Other nonthrombocytopenic purpura"
},
{
"code": "D69.3",
"display": "Immune thrombocytopenic purpura"
},
{
"code": "D69.41",
"display": "Evans syndrome"
},
{
"code": "D69.42",
"display": "Congenital and hereditary thrombocytopenia purpura"
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{
"code": "D69.49",
"display": "Other primary thrombocytopenia"
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{
"code": "D69.51",
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{
"code": "D69.59",
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{
"code": "D69.6",
"display": "Thrombocytopenia, unspecified"
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{
"code": "D69.8",
"display": "Other specified hemorrhagic conditions"
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{
"code": "D69.9",
"display": "Hemorrhagic condition, unspecified"
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FHIR