Combined immunodeficiency: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle = | | OldDxArticle =Immunological problems | ||
| CurrentStatus = | | CurrentStatus = reconciled | ||
| InitialEditorAssigned = Elaine Nagy | | InitialEditorAssigned = Elaine Nagy | ||
}} | }} | ||
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== Additional Info == | == Additional Info == | ||
incl SCID | incl SCID | ||
*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]] | *[[Immunodeficiency due to antibody deficiency or defect, hereditary or acquired]] | ||
Revision as of 13:19, 28 March 2018
| 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: | |
| Data Dependencies(Reports/Indicators/Data Elements): | No results |
| External ICD10 Documentation | |
This diagnosis is a part of ICD10 collection.
Additional Info
incl SCID
- 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
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