Combined immunodeficiency: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
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| InitialEditorAssigned = Elaine Nagy | | InitialEditorAssigned = Elaine Nagy | ||
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{{ICD10 category|Heme/immunology}} | |||
== Additional Info == | == 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 == | == 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 == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
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