ValueSet-2.16.840.1.113762.1.4.1248.23

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1248.23
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1248.23
version20221006
statusactive
publisherAmerican Institutes for Research Steward
nameCoagulationDisorders
titleCoagulation Disorders
date2022-10-06T01:02:26-04:00
experimentalfalse
descriptionICD-10-CM codes for coagulation disorders, based on AHRQ's PSI- 09 'Coagulation Disorders' code list.
Usages(none)

This value set contains 34 concepts

Code System Display
   D47.3 http://hl7.org/fhir/sid/icd-10-cm Essential (hemorrhagic) thrombocythemia
   D61.09 http://hl7.org/fhir/sid/icd-10-cm Other constitutional aplastic anemia
   D61.1 http://hl7.org/fhir/sid/icd-10-cm Drug-induced aplastic anemia
   D61.2 http://hl7.org/fhir/sid/icd-10-cm Aplastic anemia due to other external agents
   D61.3 http://hl7.org/fhir/sid/icd-10-cm Idiopathic aplastic anemia
   D61.810 http://hl7.org/fhir/sid/icd-10-cm Antineoplastic chemotherapy induced pancytopenia
   D61.811 http://hl7.org/fhir/sid/icd-10-cm Other drug-induced pancytopenia
   D61.818 http://hl7.org/fhir/sid/icd-10-cm Other pancytopenia
   D61.82 http://hl7.org/fhir/sid/icd-10-cm Myelophthisis
   D61.89 http://hl7.org/fhir/sid/icd-10-cm Other specified aplastic anemias and other bone marrow failure syndromes
   D61.9 http://hl7.org/fhir/sid/icd-10-cm Aplastic anemia, unspecified
   D65 http://hl7.org/fhir/sid/icd-10-cm Disseminated intravascular coagulation [defibrination syndrome]
   D66 http://hl7.org/fhir/sid/icd-10-cm Hereditary factor VIII deficiency
   D67 http://hl7.org/fhir/sid/icd-10-cm Hereditary factor IX deficiency
   D68.0 http://hl7.org/fhir/sid/icd-10-cm Von Willebrand disease
   D68.1 http://hl7.org/fhir/sid/icd-10-cm Hereditary factor XI deficiency
   D68.2 http://hl7.org/fhir/sid/icd-10-cm Hereditary deficiency of other clotting factors
   D68.311 http://hl7.org/fhir/sid/icd-10-cm Acquired hemophilia
   D68.312 http://hl7.org/fhir/sid/icd-10-cm Antiphospholipid antibody with hemorrhagic disorder
   D68.318 http://hl7.org/fhir/sid/icd-10-cm Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
   D68.32 http://hl7.org/fhir/sid/icd-10-cm Hemorrhagic disorder due to extrinsic circulating anticoagulants
   D68.4 http://hl7.org/fhir/sid/icd-10-cm Acquired coagulation factor deficiency
   D68.8 http://hl7.org/fhir/sid/icd-10-cm Other specified coagulation defects
   D68.9 http://hl7.org/fhir/sid/icd-10-cm Coagulation defect, unspecified
   D69.1 http://hl7.org/fhir/sid/icd-10-cm Qualitative platelet defects
   D69.3 http://hl7.org/fhir/sid/icd-10-cm Immune thrombocytopenic purpura
   D69.41 http://hl7.org/fhir/sid/icd-10-cm Evans syndrome
   D69.42 http://hl7.org/fhir/sid/icd-10-cm Congenital and hereditary thrombocytopenia purpura
   D69.49 http://hl7.org/fhir/sid/icd-10-cm Other primary thrombocytopenia
   D69.51 http://hl7.org/fhir/sid/icd-10-cm Posttransfusion purpura
   D69.59 http://hl7.org/fhir/sid/icd-10-cm Other secondary thrombocytopenia
   D69.6 http://hl7.org/fhir/sid/icd-10-cm Thrombocytopenia, unspecified
   D69.8 http://hl7.org/fhir/sid/icd-10-cm Other specified hemorrhagic conditions
   D69.9 http://hl7.org/fhir/sid/icd-10-cm Hemorrhagic condition, unspecified

Produced 08 Sep 2023