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|Pre-ICD10 counterpart:||Immunological problems|
|APACHE Como Component:||Immunocompromised|
|APACHE Acute Component:||none|
|External ICD10 Documentation|
This diagnosis is a part of ICD10 collection.
- Severe combined immunodeficiency, SCID, also known as alymphocytosis, Glanzmann–Riniker syndrome, severe mixed immunodeficiency syndrome, and thymic alymphoplasia, 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
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