Combined immunodeficiency: Difference between revisions

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 {{ICD10 transition status
-| OldDxArticle =| CurrentStatus = manually added for testing
+| OldDxArticle =Immunological problems
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Elaine Nagy
-| MinimumCombinedCodes =
 }}
 {{ICD10 dx
+| MinimumCombinedCodes =
 | ICD10 Code=D81
 | BugRequired=
 }}
+{{ICD10 category|Heme/immunology}}
-{{ICD10 category|Heme/immunology}}
 == Additional Info ==
-incl SCID
+'''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]]
-== Alternate ICD10s to consider coding instead ==
+== Candidate [[Combined ICD10 codes]] ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+== Related CCI Codes ==
-== Candidate [[Combined ICD10 codes]] ==
+{{Data Integrity Check List}}
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
 == Related Articles ==
 {{Related Articles}}
+{{ICD10 footer}}
+{{EndPlaceHolder}}