View source for Interstitial lung disease, NOS

{{ICD10 transition status
| OldDxArticle =  Pneumonitis NYD; Other respiratory problems
| CurrentStatus = reconciled
| InitialEditorAssigned = Lori Lovell
}}
{{ICD10 dx
| MinimumCombinedCodes =
| ICD10 Code=J84.9
| BugRequired= 
}}
{{ICD10 category|Infectious disease}}{{ICD10 category|Potential infection}}{{ICD10 category|Respiratory}} 

== Additional Info ==
*This code includes:
**Alveolar proteinosis
**Idiopathic pulmonary hemosiderosis
**Lipoid interstitial pneumonitis -- sometimes incorrectly called or Lipoid interstitial pneumonia
**Lymphangioleiomyomatosis (LAM)
**Histiocytosis X
**To code pulmonary fibrosis post-COVID19, combine this code with [[Post COVID-19 condition]]

{{DA | 1
This says to include
**Langerhans cell histiocytosis 
But we had a code for that, and when we retired it we stated to use [[Malignancy (clonal disorder) of blood or lymphoid tissue, NOS]] instead. Which is it? 
}}

== Alternate ICD10s to consider coding instead or in addition ==
*[[Interstitial lung disease, drug-induced (acute or chronic)]]
*[[Hypersensitivity pneumonitis (extrinsic allergic alveoliltis), NOS]]
*[[Pulmonary emphysema or bullous disease without COPD]]
*[[Fibrothorax]]

*[[Idiopathic interstitial pulmonary fibrosis]]
*[[Bronchiolitis obliterans organizing pneumonia (BOOP, cryptogenic organizing pneumonia (COP))]]

== Candidate [[Combined ICD10 codes]] ==
{{ICD10 Guideline Infection}}

== Related CCI Codes ==

{{Data Integrity Check List}}

== Related Articles ==
{{Related Articles}}


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