Interstitial lung disease, NOS: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Pneumonia| CurrentStatus = freshly automatically generated article | | OldDxArticle =Pneumonia| CurrentStatus = freshly automatically generated article | ||
| InitialEditorAssigned = Lori Lovell | | InitialEditorAssigned = Lori Lovell | ||
| MinimumCombinedCodes = | | MinimumCombinedCodes = | ||
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{{ICD10 category|Infectious disease}}{{ICD10 category|Respiratory}} | |||
== Additional Info == | == Additional Info == | ||
incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic} | incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic} | ||
Revision as of 03:10, 2017 October 16
| ICD10 Diagnosis | |
| Dx: | Interstitial lung disease, NOS |
| ICD10 code: | J84.9 |
| Pre-ICD10 counterpart: | Pneumonitis NYD, Other respiratory problems |
| Charlson/ALERT Scale: | none |
| APACHE Como Component: | Respiratory |
| APACHE Acute Component: | none |
| Start Date: | |
| Stop Date: | |
| External ICD10 Documentation | |
This diagnosis is a part of ICD10 collection.
Additional Info
incl alveolar proteinosis, idiopathic pulmonary hemosiderosis, lipoid interstitial pneumonitis, lymphangioleiomyomatosis, Histiocytosis X, Langerhans cell histiocytosis {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
Alternate ICD10s to consider coding instead
(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.) {sc:IPF, UIP, DIP, NSIP, AIP, BOOP, COP, eosinophilic}
Candidate Combined ICD10 codes
(put links to likely candidates coded with this one, eg. a cause for a trauma.)