Z83.2
BillableFamily history of dis of the bld/bld-form org/immun mechnsm
Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- FH: Blood disorder160316001
- Family history of blood disorder160316001
- Family history: Blood disorder160316001
- FH: Hereditary spherocytosis160318000
- Family history of hereditary spherocytosis160318000
- Family history: Hereditary spherocytosis160318000
- FH: Thalassaemia160319008
- FH: Thalassemia160319008
- Family history of thalassaemia160319008
- Family history of thalassemia160319008
- Family history: Thalassaemia160319008
- Family history: Thalassemia160319008
- FH: Sickle cell anaemia160320002
- FH: Sickle cell anemia160320002
- Family history of sickle cell anaemia160320002
- Family history of sickle cell anemia160320002
- Family history: Sickle cell anaemia160320002
- Family history: Sickle cell anemia160320002
- FH: Sickle cell trait160321003
- Family history of sickle cell trait160321003
- Family history: Sickle cell trait160321003
- FH: Anaemia266888008
- FH: Anemia266888008
- Family history: Anaemia266888008
- Family history: Anemia266888008
- FH: Haemophilia266889000
- FH: Hemophilia266889000
- Family history of haemophilia266889000
- Family history of hemophilia266889000
- Family history: Haemophilia266889000
- Family history: Hemophilia266889000
- Spouse haemophiliac275113000
- Spouse hemophiliac275113000
- FH: Addisonian anaemia297243001
- FH: Addisonian anemia297243001
- Family history of pernicious anaemia297243001
- Family history of pernicious anemia297243001
- FH: Autoimmune disease300933005
- Family history: Autoimmune disease300933005
- FH: Spherocytosis308746008
- Family history: Spherocytosis308746008
- Family history of rheumatic fever430777009
- Family history of sarcoidosis430778004
- Family history of disorder of immune function737367001
- Partner has haemophilia1252662002
- Partner has hemophilia1252662002
- Family history of Factor V Leiden mutation14560001000004102
- Family history of Von Willebrand disease64521000119100
- Family history of von Willebrand disorder64521000119100
- Family history of alpha thalassaemia64431000119101
- Family history of alpha thalassemia64431000119101
- Family history of anticardiolipin syndrome3340001000004108
- Family history of antiphospholipid syndrome3340001000004108
- Family history of antithrombin III deficiency108891000119103
- Family history of asplenia3470001000004103
- Family history of congenital absence of spleen3470001000004103
- Family history of splenic absence3470001000004103
- Family history of beta thalassaemia64371000119105
- Family history of beta thalassemia64371000119105
- Family history of bleeding disorder108801000119109
- Family history of blood coagulation disorder108801000119109
- Family history of congenital immunodeficiency50050161000188101
- Family history of congenital immunodeficiency disease50050161000188101
- Family history of disorder due to sex chromosome abnormality286501000119106
- Family history of erythrocytosis3490001000004106
- Family history of polycythemia3490001000004106
- Family history of factor V deficiency16400001000004104
- Family history of haemoglobin E disease64391000119106
- Family history of haemoglobinopathy E64391000119106
- Family history of hemoglobin E disease64391000119106
- Family history of hemoglobinopathy E64391000119106
- Family history of haemoglobinopathy64501000119109
- Family history of hemoglobinopathy64501000119109
- Family history of hemoglobinopathy C64381000119108
- Family history of hemophilia A6800001000004106
- Family history of hereditary factor VIII deficiency6800001000004106
- Family history of hypercoagulability130771000119102
- Family history of hypercoagulable state130771000119102
- Family history of immunodeficiency456591000124108
- Family history of immunodeficiency disorder456591000124108
- Family history of protein C deficiency109001000119105
- Family history of protein C resistance109011000119108
- Family history of protein S deficiency108981000119107
Frequently Asked Questions
What is ICD-10 code Z83.2?
ICD-10-CM code Z83.2 represents "Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism". It is a billable/specific code that can be used on a claim.
Is Z83.2 a billable code?
Yes, Z83.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z83.2 in?
Z83.2 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What SNOMED CT codes does Z83.2 map to?
Z83.2 maps to 36 SNOMED CT concepts: 297243001, 266888008, 300933005, 160316001, 266889000, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z83.2?
Z83.2 is linked to 2 UMLS Concept Unique Identifiers: C2911318, C0496715. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.