Disorder of the immune system, NOS: Difference between revisions

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{{ICD10 transition status
{{ICD10 transition status
| OldDxArticle =| CurrentStatus = manually added for testing
| OldDxArticle =Immunological problems
| CurrentStatus = reconciled
| InitialEditorAssigned = Elaine Nagy
| InitialEditorAssigned = Elaine Nagy
| MinimumCombinedCodes =
}}
}}
{{ICD10 dx
{{ICD10 dx
| MinimumCombinedCodes =
| ICD10 Code=D89.9
| ICD10 Code=D89.9
| BugRequired=  
| BugRequired=  
}}
}}
{{ICD10 category|Heme/immunology}}


{{ICD10 category|Heme/immunology}}
== Additional Info ==
== Additional Info ==
'''Includes'''
* Adult-onset Still's Disease
* Antisynthetase syndrome
* Autoimmune disorders/autoimmune diseases
* Mast cell activation disorder
* Multisystem inflammatory syndrome in children (MIS-C) for COVID 19 related link with [[Post COVID-19 condition]]
* Pemphigus vulgaris
* VEXAS syndrome- VEXAS syndrome is an adult-onset autoinflammatory disease primarily affecting males, caused by a somatic mutation of the UBA1 gene in hematopoietic progenitor cells. The name VEXAS is an acronym deriving from the core features of disease:
**V: Vacuoles are often identified in the bone marrow stem cells of patients presenting with VEXAS.
**E: The E1 ubiquitin conjugating enzyme encoded by the UBA1 gene is mutated in patients.
**X: The mutated UBA1 gene is located on the X-chromosome and thus the disease is almost exclusively found in individuals with XY chromosomes and thus said to be X-linked.
**A: Patients with VEXAS present with a wide array of Autoinflammatory conditions
**S: The mutations which cause VEXAS are Somatic, meaning that they are acquired throughout life, not inherited, and unable to be passed onto one's offspring.
* Evans syndrome
* IgG4 disease
* Immune dysregulation disorder


== Alternate ICD10s to consider coding instead or in addition ==
*[[Immune reconstitution syndrome]]
*[[Combined immunodeficiency]]
*[[Common variable immunodeficiency (CVID)]]
*[[Immunodeficiency state, NOS]]
*[[Immunodeficiency due to antibody deficiency or defect, hereditary or acquired]]
== Candidate [[Combined ICD10 codes]] ==


== Alternate ICD10s to consider coding instead ==
== Related CCI Codes ==
(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)


 
{{Data Integrity Check List}}
== Candidate [[Combined ICD10 codes]] ==
(put links to likely candidates coded with this one, eg. a cause for a trauma.)


== Related Articles ==
== Related Articles ==
{{Related Articles}}
{{Related Articles}}
{{ICD10 footer}}
{{EndPlaceHolder}}

Latest revision as of 10:27, 2024 January 18

ICD10 Diagnosis
Dx: Disorder of the immune system, NOS
ICD10 code: D89.9
Pre-ICD10 counterpart: Immunological problems
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • D89.9
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories

Additional Info

Includes

  • Adult-onset Still's Disease
  • Antisynthetase syndrome
  • Autoimmune disorders/autoimmune diseases
  • Mast cell activation disorder
  • Multisystem inflammatory syndrome in children (MIS-C) for COVID 19 related link with Post COVID-19 condition
  • Pemphigus vulgaris
  • VEXAS syndrome- VEXAS syndrome is an adult-onset autoinflammatory disease primarily affecting males, caused by a somatic mutation of the UBA1 gene in hematopoietic progenitor cells. The name VEXAS is an acronym deriving from the core features of disease:
    • V: Vacuoles are often identified in the bone marrow stem cells of patients presenting with VEXAS.
    • E: The E1 ubiquitin conjugating enzyme encoded by the UBA1 gene is mutated in patients.
    • X: The mutated UBA1 gene is located on the X-chromosome and thus the disease is almost exclusively found in individuals with XY chromosomes and thus said to be X-linked.
    • A: Patients with VEXAS present with a wide array of Autoinflammatory conditions
    • S: The mutations which cause VEXAS are Somatic, meaning that they are acquired throughout life, not inherited, and unable to be passed onto one's offspring.
  • Evans syndrome
  • IgG4 disease
  • Immune dysregulation disorder

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

Related Articles

Related articles:


Show all ICD10 Subcategories

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