Disorder of the immune system, NOS: Difference between revisions

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== Additional Info ==
== Additional Info ==
Includes:  
Includes:  
* adult-onset Still's Disease
* antisynthetase syndrome
* autoimmune disorders/autoimmune diseases  
* autoimmune disorders/autoimmune diseases  
* adult-onset Still's Disease
* mast cell activation disorder
* multisystem inflammatory syndrome in children (MIS-C) for COVID 19 related link with [[Post COVID-19 condition]]
* multisystem inflammatory syndrome in children (MIS-C) for COVID 19 related link with [[Post COVID-19 condition]]
* Antisynthetase syndrome
* 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:
* 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.
**V: Vacuoles are often identified in the bone marrow stem cells of patients presenting with VEXAS.
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**A: Patients with VEXAS present with a wide array of Autoinflammatory conditions
**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.
**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.
* pemphigus vulgaris
* mast cell activation disorder


== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==

Revision as of 16:00, 2023 May 24

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.

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

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