Diagnosis Code

J84.03 IDIOPATHIC PULMONARY HEMOSIDEROSIS


Code Information

Diagnosis Code: J84.03

Short Description: Idiopathic pulmonary hemosiderosis

Long Description: Idiopathic pulmonary hemosiderosis

The code J84.03 is VALID for claim submission

Code Classification:

  • Diseases of the respiratory system (J00–J99)
    • Other respiratory diseases principally affecting the interstitium (J80-J84)
      • Other interstitial pulmonary diseases (J84)
        • J84.03 Idiopathic pulmonary hemosiderosis

This code is valid for manifestation diagnoses

Code Version: 2022 ICD-10-CM


Synonyms

  • Hemosiderosis
  • Idiopathic pulmonary hemosiderosis

Diagnostic Related Group(s)

The code J84.03 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Interstitial Lung Disease With Mcc (196)
  • Interstitial Lung Disease With Cc (197)
  • Interstitial Lung Disease Without Cc/mcc (198)

References to Index of Diseases and Injuries

The code J84.03 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Essential brown induration of lung
  • Type 1 Excludes Notes:
    • acute idiopathic pulmonary hemorrhage in infants [AIPHI] (@R04.81*)
  • Code First:
    • underlying disease, such as:
    • disorders of iron metabolism (@E83.1*-)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
J84.03 Right Arrow 516.1 Idio pulm hemosiderosis

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
J84 Other interstitial pulmonary diseases
J84.0 Alveolar and parieto-alveolar conditions
J84.01 Alveolar proteinosis
J84.02 Pulmonary alveolar microlithiasis
J84.09 Other alveolar and parieto-alveolar conditions
J84.1 Other interstitial pulmonary diseases with fibrosis
J84.10 Pulmonary fibrosis, unspecified
J84.11 Idiopathic interstitial pneumonia
J84.111 Idiopathic interstitial pneumonia, not otherwise specified
J84.112 Idiopathic pulmonary fibrosis
J84.113 Idiopathic non-specific interstitial pneumonitis
J84.114 Acute interstitial pneumonitis
J84.115 Respiratory bronchiolitis interstitial lung disease
J84.116 Cryptogenic organizing pneumonia
J84.117 Desquamative interstitial pneumonia
J84.17 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
J84.170 Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere
J84.178 Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere
J84.2 Lymphoid interstitial pneumonia
J84.8 Other specified interstitial pulmonary diseases
J84.81 Lymphangioleiomyomatosis
J84.82 Adult pulmonary Langerhans cell histiocytosis
J84.83 Surfactant mutations of the lung
J84.84 Other interstitial lung diseases of childhood
J84.841 Neuroendocrine cell hyperplasia of infancy
J84.842 Pulmonary interstitial glycogenosis
J84.843 Alveolar capillary dysplasia with vein misalignment
J84.848 Other interstitial lung diseases of childhood
J84.89 Other specified interstitial pulmonary diseases
J84.9 Interstitial pulmonary disease, unspecified


This page was last updated on: 10/1/2023