Edit ICD10 dx: Combined immunodeficiency

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{{ICD10 transition status | OldDxArticle =Immunological problems | CurrentStatus = reconciled | InitialEditorAssigned = Elaine Nagy }} == 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 Check List}} == Related Articles == {{Related Articles}} {{ICD10 footer}} {{EndPlaceHolder}}

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