Coagulation Disorders
activeURL
http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1248.23Copied!
Version20221006Copied!
PublisherAmerican Institutes for Research StewardDate2022-10-06T01:02:26-04:00DescriptionICD-10-CM codes for coagulation disorders, based on AHRQ's PSI- 09 'Coagulation Disorders' code list.
Purpose(Clinical Focus: The purpose of this value set is to represent concepts for coagulation disorders.),(Data Element Scope: This value set may use a model element related to Diagnosis.),(Inclusion Criteria: Includes concepts for coagulation disorders.),(Exclusion Criteria: None)
Expansion
| Code | Display | System |
|---|---|---|
| D47.3 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.09 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.1 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.2 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.3 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.810 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.811 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.818 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.82 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.89 | http://hl7.org/fhir/sid/icd-10-cm | |
| D61.9 | http://hl7.org/fhir/sid/icd-10-cm | |
| D65 | http://hl7.org/fhir/sid/icd-10-cm | |
| D66 | http://hl7.org/fhir/sid/icd-10-cm | |
| D67 | http://hl7.org/fhir/sid/icd-10-cm | |
| D68.0 | http://hl7.org/fhir/sid/icd-10-cm | |
| D68.1 | http://hl7.org/fhir/sid/icd-10-cm | |
| D68.2 | http://hl7.org/fhir/sid/icd-10-cm | |
| D68.311 | http://hl7.org/fhir/sid/icd-10-cm | |
| D68.312 | http://hl7.org/fhir/sid/icd-10-cm | |
| D68.318 | http://hl7.org/fhir/sid/icd-10-cm |
systemhttp://hl7.org/fhir/sid/icd-10-cm
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"display" : "Hereditary deficiency of other clotting factors",
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"code" : "D68.311",
"display" : "Acquired hemophilia",
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"code" : "D68.312",
"display" : "Antiphospholipid antibody with hemorrhagic disorder",
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"code" : "D68.4",
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"code" : "D68.8",
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"code" : "D69.3",
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"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"code" : "D69.41",
"display" : "Evans syndrome",
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}, {
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"code" : "D69.42",
"display" : "Congenital and hereditary thrombocytopenia purpura",
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