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
Excludes 2
Conditions not included here, but the patient may have both
Code Also
A second code may be required; sequencing depends on circumstances
Related Codes(7)
Z83.0Family history of human immunodeficiency virus [HIV] disease
Z83.1Family history of other infectious and parasitic diseases
Z83.3Family history of diabetes mellitus
Z83.4Family history of endo, nutritional and metabolic diseases
Z83.5Family history of eye and ear disorders
Z83.6Family history of other diseases of the respiratory system
Z83.7Family history of diseases of the digestive system
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(170)
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
UMLS
Clinical Terms
- Family history of bleeding disorder
- Family history of sickle cell anemia
- Family history: Anemia
- Family history of haemoglobin E disease
- Family history of congenital immunodeficiency disease
- Family history of antiphospholipid syndrome
- Family history of alpha thalassaemia
- Partner has hemophilia
- Family history of asplenia
- Family history of hypercoagulability
- Family history of thalassemia
- Family history of protein C resistance
- Family history of immunodeficiency
- Conditions classifiable to D50-D89
- Family history of antithrombin III deficiency
- Family history of hemophilia
- Family history of pernicious anaemia
- Family history of haemoglobinopathy E
- Family history of thalassaemia
- FH: Spherocytosis
- FH: Hemophilia
- Family history of beta thalassaemia
- Family history of congenital absence of spleen
- Family history: Anaemia
- Family history: Blood disorder
- Family history of hemophilia A
- Family history: Hemophilia
- FH: Anaemia
- Family history: Hereditary spherocytosis
- FH: Thalassaemia
- Family history of Factor V Leiden mutation
- FH: Sickle cell anemia
- Family history of haemoglobinopathy
- Family history of sarcoidosis
- Family history of pernicious anemia
- FH: Anemia
- Family history of hemoglobinopathy E
- Family history of factor V deficiency
- Family history of haemophilia
- Family history of von Willebrand disorder
- Family history of polycythemia
- Family history of hemoglobinopathy C
- FH: Blood disorder
- Family history of protein C deficiency
- Family history: Autoimmune disease
- Family history of disorder due to sex chromosome abnormality
- Family history of hemoglobinopathy
- Family history of alpha thalassemia
- Family history of immunodeficiency disorder
- Family history of rheumatic fever
- Spouse hemophiliac
- Family history: Thalassemia
- Family history of anticardiolipin syndrome
- Family history of blood coagulation disorder
- Family history of hypercoagulable state
- Family history of erythrocytosis
- FH: Hereditary spherocytosis
- Family history of blood disorder
- FH: Autoimmune disease
- Family history: Spherocytosis
- FH: Addisonian anaemia
- FH: Sickle cell trait
- Family history of beta thalassemia
- Family history of hereditary factor VIII deficiency
- FH: Addisonian anemia
- FH: Thalassemia
- Family history: Sickle cell anaemia
- Family history of protein S deficiency
- Spouse haemophiliac
- Family history: Haemophilia
- Family history of congenital immunodeficiency
- Family history of hemoglobin E disease
- Family history of Von Willebrand disease
- Family history of hereditary spherocytosis
- Family history: Thalassaemia
- Family history: Sickle cell trait
- FH: Haemophilia
- Family history of splenic absence
- Partner has haemophilia
- Family history of sickle cell anaemia
- Family history: Sickle cell anemia
- Family history of sickle cell trait
- Family history of disorder of immune function
- FH: Sickle cell anaemia
Frequently Asked Questions
What is the ICD-10 code for family history of dis of the bld/bld-form org/immun mechnsm?
The ICD-10-CM code for family history of dis of the bld/bld-form org/immun mechnsm is Z83.2. The full clinical description is "Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism". Z83.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z83.2 mean?
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 classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and 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.
How does Z83.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like family history of dis of the bld/bld-form org/immun mechnsm affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Z83.2?
Z83.2 maps to the ICD-11 code: QC62 (Family history of diseases of the blood or blood-forming organs).
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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.