Combined immunodeficiency
ICD10 Diagnosis | |
Dx: | Combined immunodeficiency |
ICD10 code: | D81 |
Pre-ICD10 counterpart: | Immunological problems |
Charlson/ALERT Scale: | none |
APACHE Como Component: | Immunocompromised |
APACHE Acute Component: | none |
Start Date: | |
Stop Date: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
Additional Info
Includes
- Severe combined immunodeficiency, SCID, also known as alymphocytosis, Glanzmann–Riniker syndrome, severe mixed immunodeficiency syndrome, and thymic alymphoplasia,[1] is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in heterogeneous clinical presentations.
Alternate ICD10s to consider coding instead or in addition
- Immunodeficiency due to antibody deficiency or defect, hereditary or acquired
- Common variable immunodeficiency (CVID)
- Immunodeficiency state, NOS
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
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